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View my account settingsResorbable porous ceramics derived from chemically converted corals have been used successfully as bone graft substitutes for many years. Converted corals provide a 3D porous architecture that resembles cancellous bone with a pore diameter of 200–700 μm. The success of these corals as a bone graft substitute relies on vascular ingrowth, differentiation of osteoprogenitor cells, remodelling and graft resorption occurring together with host bone ingrowth into the porous microstructure or voids left behind during resorption. The resorption rate of the coral can be controlled by partial conversion to provide a hydroxyapatite (HA) layer via thermal modification. This study examined the resorption rates and bone formation of partially converted corals in a bilateral metaphyseal defect model.
Bilateral defects (5 mm x 15 mm) were created 3 mm below the joint line in the proximal tibia of 41 skeletally mature New Zealand white rabbits following ethical approval. Two variations of a calcium carbonate–HA coral (Pro Osteon 200 R, Interpore-Cross International, Irvine, CA) were examined with different HA thickness (200R; 14% or 200 RT; 28%). Empty defects (negative control) or defects filled with morcellised bone autograft from the defect sites (positive control) were performed. The tibiae were harvested at 6, 12, 24, 36 or 52 weeks, radiographed (standard x-rays and faxitron) in the anteroposterior and lateral planes. Tibias were processed for torsional testing and quantitative histomorphometry using back scattering scanning electron microscopy. Four additional rabbits were killed at time zero to determine the mechanical properties of the intact tibia (n=6 tibias) and 2 for tibias for time zero histomorphometry. Data were analysed using a 3-way analysis of variance.
No clinical complications were encountered in this study. Radiographic assessment revealed a progression in healing, implant resorption and bone infiltration. Cortical closure in the 200 R and 200RT treated defects was noted by 24 weeks. All specimens failed in torsional testing with a spiral fracture initiating at the distal defect site and extending into the distal diaphysis. Torsional properties reached intact control tibia levels by 24 weeks in both groups. No significant differences were noted between 200 R and 200 RT based on torsional data. SEM revealed progressive resorption of the calcium carbonate core of the 200 R and 200 RT with time, infiltration of bone and ingrowth to the HA layers. Time and measurement site (cortical versus cancellous) were significant for implant resorption, bone, and void. The thinner HA layer (200 R) resorbed more quickly compared to the thicker layer (200 RT) in the canal as well as cortical sites. Increased bone and decreased void were noted at the cortex measurement sites in the 200 R group at 24 weeks and in the 200 RT group at 12 and 24 weeks (p< 0.05). Implants were nearly completely resorbed by 52 weeks with only a few percent of implant remaining.
Chondromodulin-I (ChM-I) is a bifunctional autocrine regulator of cartilage, initially isolated from fetal bovine epiphyseal cartilage
In 2-week old rats, ChM-I was synthesised by all epiphyseal chondrocytes and strong immunostaining was found in the matrix. In the growth plates, ChM-I staining was present in chondrocytes and matrix of the reserve, proliferating and maturing zones with loss of staining in the hypertrophic zone. However, ChM-I was also present where cartilage canals had penetrated into the chondroepiphysis. In 4–16 week old rats, there was a progressive change in the localisation of ChM-I. Hypertrophic chondrocytes also became positive for ChM-I, while cellular staining gradually disappeared from the other zones. By 12–16 weeks, very strong immunostaining was present almost exclusively on the inner perimeter of the lacunae of hypertrophic chondrocytes. As lacunae were opened at the vascular front, ChM-I initially remained on the cartilage-side of the lacunae, and then disappeared completely. In aged rats, very little ChM-I was present in the cells and matrix of the growth plates, except where remodelling had occurred or chondrocytes had become re-activated.
The rate of longitudinal growth in rats is high between 1–5 weeks, then declines until skeletal maturity at approximately 12 weeks, after which a very slow rate of growth continues until 26 weeks. In young rats, the loss of ChM-I in the hypertrophic zone was as expected for an anti-angiogenic factor, i.e. loss was required before vascular invasion could take place. However, the same did not apply to cartilage canal formation, since there was no loss of ChM-I around cartilage canals. The change in the localisation of ChM-I in mature rats, in particular the very intense immunolocalisation around hypertrophic chondrocytes, might be related to the reduced rate of growth. It is possible that rapid vascular invasion must be slowed down in these growth plates and that ChM-I prevented vascular invasion until degraded by proteases, such as MMP-9.
The relative absence of ChM-I in the stationary growth plates of aged rats suggests that other anti-angiogenic factors prevent vascular invasion in these growth plates.
Osteoblast progenitor cells can be isolated from human bone marrow and on an appropriate carrier following differentiation into osteoblasts a bone block could be formed. This supply of autologous, osteoinductive bone graft substitute would have significant implications for clinical use. The aim of the study was to assess whether osteoblast progenitor cells isolated from human bone marrow, seeded onto porous hydroxyapatite (HA) blocks adhere, proliferate and differentiate into osteoblasts under the influence of HA alone.
After informed consent, bone marrow was aspirated from the iliac crest of 8 patients. The osteoblast progenitor cells were separated from the haematological cells and cultured in vitro. Evidence for the osteoblast progenitor nature of the cells was obtained by adding osteogenic supplements: dexamethasone, ascorbic acid and b-glycophosphate, and comparing alkaline phosphatase (ALP) and osteocalcin expression with that of unstimulated cells. Undifferentiated osteoblast progenitor cells were seeded at a density of 2x10 6 cells/porous HA cylindrical block (8 x 8 x10 mm). The cell adhesion to the HA was observed, and proliferation and ALP expression was measured over 15 days.
In monolayer culture the isolated bone marrow cells were morphologically identified as mesenchymal stem cells. When osteogenic supplements were added the phenotype became consistent with the morphology of osteoblastic cells, and the ALP expression was significantly higher (P< 0.05) after 5 days in culture compared with cells that had not been stimulated to differentiate.
On the HA osteoblast progenitor cells were adherent and became more osteoblastic, being separated from the HA surface by an osteoid matrix layer on electron microscopy. The ALP expression by these cells increased significantly (P< 0.05) over the 15 day culture period.
Bone marrow contains mesenchymal stem cells with osteogenic potential that are known as osteoblast progenitor cells. In this study we have shown that osteoblast progenitor cells can be isolated from human bone marrow and will adhere to and proliferate on HA blocks in vitro, and differentiate into osteoblasts spontaneously under the influence of the HA scaffold. These constructs could be used as osteoinductive bone grafts.
Deep infection is a devastating complication of total joint arthroplasty. In a significant proportion of cases it remains a diagnostic challenge. Haematological tests are not specific, particularly in chronic cases, and radiological investigations such as bone scan and radiographs are of only limited value. The most common infective organisms are staphylococcus and some streptococcus species. Acidity is a well established occurrence in infective processes and is caused by the direct production of acid by the organism or by enzymatic degradation of tissues
Nineteen consecutive patients undergoing either revision total knee replacement (TKR) or arthroscopic synovial biopsy were included in the study. All had had their primary joint replacement within the previous 3 years. All had a painful total knee replacement and some had evidence of loosening of the prosthesis on radiological investigations. The following investigations were performed on each patient, White cell count (WCC), Erythrocyte Sedimentation Rate (ESR), C-Reactive Protein (CRP), interface synovial biopsy for histology and microbiology and a synovial fluid aspiration from the affected joint prior to application of a tourniquet. A blood gas analyser was used to measure pH, pCO2, pO2, Lactate and Glucose in all synovial fluid specimens.
Seven patients were diagnosed as having an infected TKR on clinical and laboratory investigations. The mean synovial fluid biochemistry results were pH = 7.09, pO2= 5.08kPa, pCO2=10.40kPa, Lactate = 5.33 mmol/l, Glucose = 2.30 mmol/l. In the non-infected group the results were pH = 7.23, pO2 = 7.72kPa, pCO2 = 8.41kPa, Lactate = 4.03 mmol/l, Glucose = 3.42 mmol/l. The differences in pH, pCO2/pO2 ratio, and glucose levels were statistically significant (t-Test p < 0.05) between the two groups. Lactate levels were not significantly different. There was no correlation between high WCC’s and synovial fluid biochemistry or laboratory results for infected cases. Using laboratory results as a gold standard and a synovial fluid pH of less than 7.20, the sensitivity was 85% and specificity 77% for diagnosing an infection. Using a combination of the synovial fluid biochemistry results these values were greater.
Synovial fluid biochemistry is significantly altered in infected total knee replacements. pH levels below 7.2, pCO2/pO2 ratio above 2.5 and Glucose levels below 2.5 mmol/l are strong indicators of an infected TKR. Synovial pH assessment may prove to be a quick, cheap and effective method of diagnosing an infected TKR and may also apply to other joints. Further studies using non-problematic TKR’s as controls are required.
Ex vivo gene transfer of osteogenic factors into multipotential stem cells offers potentially important therapeutic implications in a variety of musculoskeletal diseases. One possible approach is the development of a cellular vehicle, namely bone morphogenetic protein (BMP)-producing bone marrow cells, created using adenoviral gene transfer. These transduced cells provide local delivery of BMP for bone formation. The aims of this study were to study the feasibility of gene transfer to human bone osteoprogenitor cells, using adenoviral vectors. Specifically, the aims were to study the efficacy of transduction with an adenoviral vector expressing BMP-2 and then to determine the ability of the transduced cells to produce active BMP-2 and to generate bone ex vivo.
Primary human bone marrow osteoprogenitor cells were expanded in culture and infected with AxCALacZ, a replication-deficient adenoviral vector carrying the
To examine whether adenoviral transfection affected the osteoblast phenotype and their ability to mineralise in vitro, adenovirally-transduced bone marrow cells expressing BMP-2 were seeded onto poly(-lactic acid
These results indicate the ability to deliver active BMP-2 using human bone marrow osteoprogenitor cells following adenoviral infection. The maintenance of osteoblast phenotype in extended culture and generation of mineralised 3-D scaffolds containing such constructs offers a realistic approach to tissue engineer bone for orthopaedic applications.
Detection of infection in total joint replacements (TJR) is notoriously difficult. Ideally the diagnosis should be known before revision arthroplasty is undertaken. The level of C-reactive protein (CRP) is one readily available test. Sanzen et al. reported sensitivity of 78% and specificity of 100% for CRP in distinguishing infection in 23 infected TJRs and 33 non-infected TJRs undergoing revision, using a cut off of 2mg/dl
The results of CRP and the operative investigations of 26 patients undergoing revision arthroplasty (15 hips and 11 knees) were studied prospectively. In our unit CRP is assayed in mg/dl serum by an automated machine. During revision arthroplasty, multiple specimens were taken from around the joint for microbiological and histological examination. Microbiological cultures were carried out on solid media and broth in aerobic and anaerobic conditions. Histological analysis assessed the level of neutrophils present in the tissue. The presence or absence of pus was noted. The results were analysed graphically and a cut off level of CRP was then chosen for analysis of reliability.
Thirteen patients were infected and 13 were not. Eleven of the 13 infected patients had a CRP greater than 2 mg/dl, and 10 of the 13 non-infected patients had a CRP less than 2 mg/dl. Using 2 mg/dl as a cut off, CRP had a sensitivity of 85% and a specificity of 77%. If 4mg/dl is taken as the threshold for infection, then CRP is 100% specific but only 61% sensitive.
CRP is a useful investigation in the diagnosis of infection in joint replacements. However we have shown that a cut off of 2mg/dl is not 100% specific for non-infected patients. Increasing the threshold improves the specificity, but reduces the sensitivity. Unfortunately there is no single investigation that is 100% accurate in this setting. CRP results must be interpreted in the light of the clinical picture and other investigations. These patients are part of an ongoing study to identify the most reliable criteria for diagnosing the presence of infection in total joint replacement.
The formation of biomimetic environments using scaffolds containing cell recognition sequence and osteo-inductive factors in combination with bone cells offers tremendous potential for bone and cartilage regeneration. In tissues, collagen forms the scaffold by mediating the flux of chemical and mechanical stimuli. Recently, a synthetic 15-residue peptide P-15, related biologically to the active domain of type I collagen, has been found to promote attachment and the osteoblast phenotype of human dermal fibroblasts and periodontal ligament fibroblasts on particulate anorganic bone mineral (ABM). The aim of this study was to exam the ability of the collagen peptide, P-15, to promote human osteoprogenitor attachment, proliferation and differentiation on cell culture surfaces and 3-D scaffolds.
Selected human bone marrow cells were cultured on particulate microporous anorganic bone mineral (‘pure ‘ hydroxyapatite based on x-ray diffraction standard JCPDS9-432) phase and polygalactin vicryl mesh adsorbed with or without P-15 in basal or osteogenic conditions. Cell adhesion, spreading and patterning were examined by light and confocal microscopy following incorporation of cell tracker green and ethidium homodimer fluorescent labels. Osteoprogenitor proliferation and differentiation was assessed by DNA content and alkaline phosphatase specific activity. Growth and differentiation on 3-D ABM structures were examined by confocal and scanning electron microscopy (SEM).
P-15 promoted human osteoprogenitor cell attachment and patterning on particulate bovine anorganic bone mineral phase and polygalactin vicryl mesh over 5–24 hours compared to culture on ABM and vicryl mesh alone as observed by photomicroscopy. Increased alkaline phosphatase specific activity was enhanced following culture on P-15 adsorbed matrices as recognized by enhanced expression of alkaline phosphatase, type I collagen, osteocalcin and cfba-1. The presence of mineralised bone matrix and extensive cell ingrowth and cellular bridging between 3-D ABM matrices and polygalactin vicryl mesh adsorbed with P-15 was observed by confocal microscopy and alizarin red staining. SEM confirmed the 3-D structure of newly formed cell constructs and cellular ingrowth on and between the P-15 modified inorganic bone mineral materials. Negligible cell growth was observed on ABM alone or polygalactin vicryl mesh alone.
These observations demonstrate that the synthetic 15-residue collagen peptide, P-15, when adsorbed to ABM or polygalactin vicryl mesh, can stimulate human osteoprogenitor attachment and spreading. They also demonstrated that P-15 coupled 3-D matrices stimulate human osteoprogenitor differentiation and materialisation. The studies indicate that a synthetic analogue of collagen provides a biomimetic environment supportive for cell differentiation and tissue regeneration and indicate a potential for the use of extracellular matrix cue in the development of biomimetic environments for bone tissue engineering.
Pre-revision detection of infection in failed total joint replacements (TJR) is essential to allow appropriate management planning. Unfortunately, low-grade infection is often difficult to detect. The use of molecular biology may offer increased sensitivity in this setting. We have analysed the use of the Polymerase Chain Reaction (PCR) to diagnose infection in pre-operative aspirates in a group of patients undergoing revision arthroplasty. We prospectively tested 50 aspirates in 50 patients with failed TJR (34 hips and 16 knees). Antibiotics were omitted for 2 weeks prior to aspiration. The aspirate was sent for microbiological culture in aerobic and anaerobic conditions. An aliquot was retained for PCR analysis which involved DNA extraction then amplification of an 882 base pair segment of the Universal 16S RNA gene. In 33 patients who subsequently underwent revision arthroplasty multiple specimens were taken from around the joint for microbiological and histological examination and the presence or absence of pus was noted. The patient was deemed to be infected if one of these criteria was found: 2 or more intra-operative cultures positive for the same organism; an acute inflammatory response on histology; pus in the joint at revision
PCR was positive in 29 cases. Aspiration microbiology was positive in 13 cases. Of the 33 cases revised, 15 patients were deemed to be infected using the previously established criteria, described above. Compared to preoperative aspiration microbiology PCR had a sensitivity of 92% and specificity of 54%. Compared to the published criteria for infection, PCR was 93% sensitive and 61% specific. If rheumatoid cases are excluded the specificity improves to 71%.
It was concluded that PCR has the ability to amplify very small amounts of target DNA. The apparently high false positive rate compared to aspiration microbiology may indicate that PCR is picking up DNA from contaminating or non-viable organisms (treated or phagocytosed), giving poor specificity. However, microbiology is known to have poor sensitivity on pre-operative aspiration samples, and some of the microbiology results may be false negative. Compared to the criteria for infection after revision our results for PCR are more encouraging, especially for non-rheumatoid patients. These patients are part of an ongoing study to identify the most reliable criteria for pre-operative diagnosis of infection in total joint replacement.
Most infections in arthroplasty are caused by staphylococci, about half being due to
Antibodies to recombinant sequences of Fnbp and Fgbp were raised in rabbits. A strain of
Each antibody reduced the number of bacteria binding to all three materials by greater than 50%. Combining the two antibodies gave similar results to those when they were used individually.
These preliminary results suggest that while further research is required, vaccination aimed at blocking bacterial attachment to conditioning film on implanted prostheses might reduce the incidence of
Fracture repair is a complex physiological process during which bone shows the remarkable ability to mount a repair process, restoring its mechanical integrity and anatomical configuration by original osseous tissue. Programmed cell death, or apoptosis, is a naturally occurring cell suicide pathway with a homeostatic function in the maintenance of continuously renewing tissues. The present study investigated the relation between cell proliferation and cell death (apoptosis) during fracture healing in a mouse femoral model.
Left femoral osteotomies were performed in 20 male CFLP mice (35–45g), immobilised with uniplanar external fixators. 4 animals were sacrificed on days 2, 4, 8, 16 and 24 post-fracture and fracture callus collected for paraffin embedding. Localisation of cell proliferation was examined using immunohistochemistry with proliferating cell nuclear antigen (PCNA) monoclonal antibody. Apoptotic cells were visualised with the terminal deoxynucleotidyl transferase (TdT)–mediated dUTP-biotin nick end-labelling (TUNEL) method. Random images of each time specific specimen were captured via a digital camera and the positive labelling indices of PCNA and TUNEL labelling were calculated and statically compared.
Cell proliferation and apoptosis were found co-existing during the entire period of fracture healing studied. Cell proliferation was predominant in the early phases of fracture healing (days 2–8). PCNA positive labelling index peaked at day 8 (p< 0.01, t-test) and PCNA-positive cells were not limited to the fracture gap mesenchymal tissues but extended in the periosteum along most of the fractured femur. TUNEL positive labelling was minimal in the early stages (days 2–8). In later stages of fracture healing (days 16–24), PCNA expression declined as intramembranous and endochondral ossification spread within the fracture site and apoptosis was the dominant cell activity with the TUNEL positive labelling index peaked at day 16 (p< 0.05, t-test) and then declined sharply at day 24.
The current study indicated that apoptosis was a normal concomitant during fracture repair, confirming programmed cell death in chondrocytes and bone cells, and that cell proliferation and apoptosis were tempero-spatially dependent. These findings support the view that apoptosis is a natural process, genetically programmed and active during fracture repair. The demonstration of a mixture of proliferative and apoptotic cell populations in the regenerating tissues of fracture callus, suggests that apoptosis and cell proliferation may be regulated by local factors during fracture healing.
Metallic implants are used frequently in the operative repair of joints and fractures in orthopaedic surgery. Metal infection is a catastrophic complication of the surgery with patients loosing their newfound mobility and independence, associated morbidity and mortality is high. Orthopaedic implant infection is chronic and biofilm based. Present treatment focuses on removing the infective substratum and implant surgically as well as prolonged anti-microbial therapy. Biofilms are 500 times more resistant than planktonic strains of bacterial flora to antibiotics, and with evolving resistant strains this form of therapy is loosing ground. Silver coatings on polymers and nylon (catheters, heart valve cuffs, burn dressings) have shown inhibition of this biofilm formation in its adhesion stage. Our aim was to deposit effective, minute, biocompatible, anti-bacterial layers of silver on orthopaedic stainless steel K-wires.
Combining magnetron sputtering with a neutral atom beam (Saddle Field) plasma source at 10−4 mbar in argon gas at temperatures of 60°C, a silver coating of 99.9% purity was deposited onto stainless steel orthopaedic K-wires. Coating thickness measurements were obtained using glancing angle x-ray diffraction of glass slides coated adjacent to wires. Magnetron parameters were modified to produce varying thickness of silver. Adhesiveness was examined using Rockwell punch tests and tape tests. Silver leaching experiments were carried out in phosphate buffered saline at 37°C for 48hrs and using inductive coupled plasma spectrometry to assess leached silver ions. Surface microscopy visualised physical changes in the coatings. Biofilm adhesion was determined by exposing wires to
K-wires were coated with 5 to 50 nm of silver by running the magnetron sputtering at low currents. These coatings showed excellent adhesive properties within the 48hr exposed with only 5% of silver leaching in buffered saline. The silver coated wires showed a log 3–4 fold reduction in biofilm formation as compared to control wires. The coatings showed no cytotoxic effects.
Silver coating of medical implants has been shown in urological catheters to reduce biofilm infection. We have perfected a method of depositing thin layers of anti-bacterial silver onto stainless steel, which is both anti-infective and biocompatible. This coating could potentially add to the armourary of anti-infective agents in the elimination of infection related orthopaedic implant failure.
During the process of distraction osteogenesis new bone is formed rapidly and undergoes remodelling almost immediately. Little is known about the regulatory mechanisms governing the removal of the redundant callus in this process. Tissue homeostasis is achieved by a delicate balance between the processes of cell death (apoptosis) and cell proliferation. The aim of this study was to test the hypothesis that apoptosis is involved during distraction osteogenesis.
Mid-tibial osteotomies were performed in 6 adult male NZW rabbits (age; 24 weeks, weight; 3.0 −3.5 kg), and the tibiae stabilised with unilateral external fixators (Orthofix M-100). 7 days later, twice daily distraction was initiated at rates of 0.7 mm/day for 3 weeks. BrdUrd (40mg/kg) was injected intravenously to the rabbit 1h before killing. The regenerate bone was collected, fixed in 10% buffered formalin and decalcified for paraffin embedding. Some fresh regenerate bone tissues were also prepared for examination under transmission electronic microscopy (TEM). BrdUrd immunohistochemistry has been used to detect proliferating cells and the terminal deoxynucleotidyl transferase (TDT)-mediated dUTP-biotin nick end-labelling (TUNEL) method was used to identify cells undergoing apoptosis. To detect bone-resorbing cells, tartrate-resistant acid phosphatase (TRAP) staining was also performed.
BrdUrd positive cells and TUNEL-positive cells were shown to coexist in most of the areas in the regenerates. In the mineralisation front, the majority of the TUNEL-positive cells were present in the transitional region between the fibrous tissue and the new bone. The TUNEL-positive cells were close to or on bone surfaces, and some of the newly formed osteocytes in the new trabeculae were also positive. The TUNEL-positive cells were also seen in the cartilage region of the regenerate. However, the TUNEL labelling was greatly reduced in the new bone close to the osteotomised bone ends, TUNEL-positive labelling were not detected in the cortical bone of the osteotomised bone ends and in the adjacent surrounding periosteum. TRAP staining in the regenerate revealed similar patterns of distribution to those of the TUNEL staining. There were more TRAP-positive cells in the new bone near the mineralisation front than in that of the new bone region, which was close to the osteotomised bone ends. TEM examinations have demonstrated characteristic signs of apoptotic changes in the fibroblast, osteoblast and osteocytes in the specific regions of the distraction regenerate.
The study provided evidence that in the process of rapid bone formation during distraction osteogenesis, superfluous cells are removed by apoptotic mechanisms. The demonstration of a mixture of proliferative and apoptotic cell populations in the regenerating tissue, indicates that apoptosis and cell proliferation may be regulated by local factors. The neovascularisation of the regenerate and withdrawal of growth factors and cytokines may be responsible for apoptosis occurring in some parts of the regenerating tissue. The changes of distribution of apoptotic cells in the different regions of the regenerate, together with the observed patterns of osteoclast activities, suggest that bone cells undergoing apoptosis may initiate rapid bone remodelling seen during distraction osteogenesis.
Atrophic non-unions are usually attributed to impaired blood supply but the events that lead to atrophic non-union remain poorly understood. Recent studies
Twenty eight adult female Wistar rats underwent application of a novel circular frame external fixator to the right tibia under general anaesthesia. The fixator construct was standardised, with eight needles that were drilled through the skin into the proximal and distal metaphyses of the tibia. An osteotomy was performed with a 1mm burr under irrigation. The periosteum was removed on 14 of the 28 animals using a scalpel and the intramedullary canal was curetted. Both insults were performed proximally and distally for a distance equivalent to 1 diameter of the tibia. A 1mm gap was introduced at the osteotomy site and the wound was closed. Once the animal had recovered it was allowed unrestricted weight bearing. Anteroposterior X rays were performed every 2 weeks. Animals were killed at 1, 3, 8 and 16 weeks. Callus areas were measured from X rays using an image analysis system. The average callus area was calculated for each rat every 2 weeks as an indicator of callus production. Specimens were fixed, decalcified, embedded in paraffin wax and 6 ìm sections were stained with H& E. Vascularity was assessed immunohistochemically with monoclonal antibody against smooth muscle actin. The total number of blood vessels in the interfragmentary gap was counted.
At 8 and 16 weeks post-osteotomy all animals where stripping and curetting had been performed went on to an atrophic non-union. All animals where this was not performed went on to unite successfully. Histological observations support these radiological findings. Significantly less callus formed in the non-unions than in those that united. There were significantly fewer vessels in the non-unions at week 1 compared to the controls but, by 8 weeks the blood vessel density in the established atrophic non-unions had reached the same level as the vessel density during normal healing.
An atrophic non-union model that closely resembles the clinical situation has been developed and validated in rats. The results support the hypothesis that the number of vessels in atrophic non-unions reaches the same level as in those that unite but at a later time point. It is concluded that diminished vessel density within the first 3 weeks may prevent fractures from uniting.
Fracture healing involves many local and systemic regulatory factors. Progress in identifying signaling events downstream has been made with the discovery of a novel family of proteins, the Smad, as TGF-ß/activins/BMPs signal transducers. Smads are the vertebrate homologs of
Eighteen 3-month old female CD-COB rats were used. A standard closed fracture was made in the mid-shaft of right femur using a 3-point bending device. The left limb served as the non-fracture control. The rats were divided into 3 groups (6 per group) and sacrificed at day 3, 10 and 28 after fracture. The femurs were harvested, fixed in buffered formalin for 48 hours and decalcified with 10% formic acid-formalin solution. The decalcified tissues were embedded in paraffin and 5μm sections were cut onto silane-coated slides. Representative slides from each block were stained with routine haematoxylin and eosin (H& E). Sections were cut for immunohistochemistry for protein marker expression by a standard procedure for Smads and BMP 4 and 7. Sections were viewed and analysed by colour video image analysis using a 40x objective, a 10x eyepiece, and a fixed frame of 128 × 128 pixels (49152.0 μm2). Ten fields per slide were examined.
Smad proteins (Smads 1, 4, and 6) were expressed during the early stages (day 3) of fracture healing by bone marrow stromal cells, osteoblasts, fibroblasts and chondrocytes located in the intramembranous and endochondral ossification regions around the fracture site. Differential expressions of individual Smads, particularly Smad 1 and Smad 6, at different time-points (Smad-1 was higher than Smad-6 at day 3, whilst Smad-6 was much higher than Smad-1 at day 10) suggest that Smad proteins are not simply BMP signal transducers. Smads may also be responsible for up- and/or down-regulation of transcriptional events during the intramembranous and endochondral ossification. Smad-4, a Co-SMAD, expression newly formed bone and cartilage suggests an additional function beyond the signal transduction in rat fracture healing. BMP-4 and BMP-7 were highly expressed at day 3 and 10. BMP-7 expression was greater than BMP-4 at day 3 but switched by day 10 (BMP-4 > BMP-7). Smads represent a new level where specific therapeutic strategies can be targeted considering the interactions with a number of BMPs.
Vascular Endothelial Growth Factor (VEGF) has been shown to stimulate angiogenesis in a number of tissues and, in addition, to possess direct vasoactive properties. Stimulation of blood flow and angiogenesis are important features of the fracture healing process, particular in the early phases of healing. Inadequate vascularity has been associated with delayed union after fracture. The periosteum, and in particular its osteogenic cambial layer, has been shown to be very reactive to fracture and to contribute substantially to fracture healing. Fracture haematoma contains a considerable concentration of VEGF and enhanced plasma levels are observed in patients with multiple trauma. VEGF has been suggested to play a role during new bone formation possibly providing an important link between hypertrophic cartilage, angiogenesis and consequent ossification. However, the expression of VEGF in normal periosteum and in periosteum close to a fracture has not been previously reported. We hypothesise that the expression of VEGF in long bone periosteum will show a distinct response to fracture.
We investigated the expression of VEGF
In Group 1 the periosteum showed abundant but delicate blood vessels staining throughout for VEGF but there was no other visible staining of other structures or cells. In Group 2 the vasculature in the periosteum close to the fracture site demonstrated a characteristic, time-dependent course of expression of VEGF. At 24 and 48h following fracture the vasculature showed a heterogenous picture. The vessels in periosteum showed signs of activation: thickened endothelia and dilated lumina, but did not express VEGF. At 60h the vessels began to show signs of the presence of VEGF protein and by 4 days most periosteal vessels expressed VEGF. Also at this time, VEGF staining was visible in some of the stromal cells of the periosteum that was not seen in any of the earlier times. At 9 days VEGF was visible not only in the omnipresent vasculature, but now consistently in spindle shaped cells of fibroblastic appearance and chondrocytes throughout the early callus.
This study, though limited by the number of patients, shows for the first time the expression of VEGF in normal periosteum as well as in periosteum during fracture healing. Interestingly, activated vessels in the early healing phase show little expression of VEGF; however it is known that the fracture haematoma contains VEGF in abundance. It is possible that the vasoactive role of VEGF prevails in these early days. There may be a critical time point at around 48h post fracture following which angiogenesis begins and VEGF is expressed in the endothelium throughout the vessel wall. The study suggests an important role for VEGF in the regulation of fracture healing. VEGF is not only expressed in endothelial cells within the periosteum but also in fibroblast-like stem cells and chondrocytes throughout the early callus suggesting it may play an important role in both osteo- and angiogenesis
In rheumatoid arthritis (RA) and other arthritic disorders e.g. gout, there is destruction of articular cartilage and juxta-articular bone. Osteoclasts are specialised multinucleated cells (MNCs) that carry out bone resorption. It has previously been shown that circulating monocytes and synovial macrophages in RA can be stimulated to differentiate into functional osteoclasts in the presence of RANKL and M-CSF. The aim of this study was to determine whether the mononuclear cells present in synovial fluid of RA patients are capable of differentiating into functional osteoclasts in the presence of osteogenic factors.
Mononuclear cells were isolated from the synovial fluid obtained from patients with Ra, osteoarthritis (OA) gout and joint trauma. The cells were seeded onto dentine slices and coverslips and cultured for up to 21 days in the presence/absence of RANKL (30ng/ml) and M-CSF (25ng/ml). Cells cultured on coverslips for 24h, 14 and 21 days were assessed for the expression of the monocyte-macrophage antigen CD14 that is known to be expressed by osteoclasts, and the osteoclast associated markers; tartrate-resistant acid phosphatase (TRAP) and vitronectin receptor (VNR). After 21 days, dentine slices were assessed for evidence of osteoclastic lacunar resorption.
After 24 h culture on coverslips mononuclear cells isolated from the synovial fluid of all the above joint conditions were largely CD14+, and entirely negative for TRAP and VNR. After 14 days culture, in the presence of RANKL and M-CSF these synovial fluid macrophages were stimulated to form multinucleated osteoclasts which were TRAP+ and VNR+ and capable of forming resorption pits on dentine slices. In the absence of either RANKL or M-CSF osteoclast formation did not occur.
The osteogenic factors RANKL and M-CSF have been shown to be present in the synovial fluid of patients with RA, OA, gout and joint trauma. Results from this study demonstrate that CD14+ mononuclear cells (macrophages) in the synovial fluid of patients with the above conditions have the capacity to differentiate into functional multinucleated osteoclasts in the presence of RANKL and M-CSF. These findings show that one cellular mechanisms whereby bone erosions many occur in arthritic disorders is through increased osteoclast formation of synovial fluid macrophages; this process requires RANKL and m-CSF, both of which are produced by inflammatory cells e.g. T Cells found in the synovial fluid and the arthritic synovial membrane.
Tibial fractures represent a heterogeneous group of fractures that are difficult to treat and vary widely in their time to union. Judging when it is safe to remove an external fixator or plaster cast requires clinical and radiological assessments both of which are subjective. Any errors in determining when a fracture has healed can lead to a prolonged treatment time or to refracture. Many methods have been employed to attempt to define clinical union in an objective manner including ultrasound, DEXA scanning, vibration analysis, and fracture stiffness measurements. Stiffness measurements are however time consuming to perform, of debatable clinical significance, and applicable only to fractures treated with external fixators. It has been previously observed
A group of ten patients with tibial fractures treated by external fixation were studied. Using a Kistler force plate set into the floor, ground reaction forces for both lower limbs (fractured and non-fractured) were measured during normal walking at three weekly intervals. Concurrent fracture stiffness measurements were made using the Orthofix Orthometer.
In 8 patients who made good recoveries, the fixator was removed between 15–20 weeks post injury when the fracture stiffness had reached a minimum of 15 Nm/deg. Weight-bearing through the injured leg was seen to approach 90% of that through the uninjured leg in the 3 weeks prior to fixator removal. Two patients with delayed union achieved weight bearing of less than 40% of normal between 15–20 weeks. They also demonstrated low values of fracture stiffness (< 5 Nm/deg.) and subsequently required operative intervention to achieve union.
In this small study of 10 patients, weight bearing appears to correlate well with clinical union. It is quicker and easier to assess than stiffness and potentially has relevance to other fixation methods. We are continuing these measurements on conservatively treated, intra-medullary nailed, and externally fixed tibial fractures.
The use of intra-articular hyaluronic acid injections for the treatment of early osteoarthritis is in widespread clinical use. Hyaluronate (HA) is a major component of connective tissue
Bovine articular chondrocytes were isolated by sequential digestion with pronase and collagenase and seeded in 2% alginate at 1x107 cells/ml. The constructs were cultured for up to 14 days in standard culture medium (DMEM + 20% Fetal calf serum) containing varying concentrations of HA (Sigma), including doses equivalent to those found in vivo. The medium was replaced every 3 days and representative constructs were removed from culture, digested and assayed for DNA, glycosaminoglycans and Collagen. Further constructs were fixed in 4% paraformaldehyde for standard histology and immunolocalisation of collagen types I, II and chondroitin-6-sulphate.
Chondrocytes cultured in the HA system proliferated (increase in DNA) at a faster rate than the controls. There was a 2.2 fold increase in cell concentration at 14 days compared to a 1.2 fold increase in the controls. Total GAG levels at each time point were significantly greater for cells cultured in HA than in controls. Histologically, constructs were characterised by extensive cell cluster formation and intense Safranin-O staining. The newly synthesised matrix also stained positive for type II collagen. By contrast, control constructs exhibited minimal cluster formation, Safranin-O and type II collagen staining.
Cells maintained with HA exhibited a significantly greater rate of proliferation and matrix production. The presence of matrix rich in type II collagen indicates maintenance of chondrocytic phenotype. By contrast, cells cultured without HA did not show these features. These results support the use of intra-articular injections for the treatment of osteoarthritis. The benefits of HA injections may be due to cellular mechanisms as well as mechanical.
The use of intra-articular corticosteroid injections for their anti-inflammatory effects is widespread amongst clinicians. Despite their use in both rheumatoid arthritis and osteoarthritis, the effect of these agents on articular chondrocytes is not fully established. Previous reports suggest a detrimental effect on cartilage explants resulting from inhibition of matrix synthesis
Bovine articular chondrocytes were isolated by sequential digestion with pronase and collagenase and seeded in 2% alginate at 1x107 cells/ml. The constructs were cultured for up to 15 days in standard culture medium (DMEM + 20% Fetal calf serum) containing varying concentrations of MP, including doses equivalent to those found in vivo. The medium was replaced every 3 days and representative constructs were removed from culture, digested and assayed for DNA and glycosaminoglycans. Further constructs were fixed in 4% paraformaldehyde for standard histology and immunolocalisation of collagen types I, II and chondroitin-6-sulphate.
Chondrocytes cultured in MP containing medium showed a significant abnormality in cell morphology compared to controls at the day 15 time point. Histologically there was evidence of cell necrosis, reduced amounts of extracellular matrix and loss of collagen type II staining. The effects were dose dependant, with significant damage occurring even at clinical doses. Biochemical analysis revealed a reduction in DNA content and an inhibition of glycosaminoglycan and collagen type II synthesis. In contrast, in the controls, there was cell proliferation with a cell doubling time of 14 days, collagen type II containing extracellular matrix synthesis occurred and the chondrocytes maintained their phenotype throughout the culture period.
Methylprednisolone has a significant detrimental effect on cultured articular chondrocytes in vitro. There was significant cell necrosis associated with inhibition of extracellular matrix synthesis. Based on these results, intra-articular corticosteroid injections should be used with extreme caution.
The ACL-deficient knee demonstrates an increase in both tibial rotation and translation that can lead to progressive degeneration within the knee joint. Functional Knee Braces (FKBs) have often been prescribed as an integral part of treatment programmes for such patients. However, the ability of a FKB to increase the stability of the ACL-deficient knee by controlling tibial translation has yet to be confirmed. In addition the athlete with ACL deficiency frequently asks if he/she can use a treadmill as a safe indoor exercise tool.
A prospective study was carried out on 15 pre-operative ACL-deficient patients and 15 fully matched subjects as controls. A gait analysis study was designed using the CODA
ACL-deficient subjects had significantly lower speed, shorter stride length and consequently longer double support time while walking on level ground (p< 0.05). None of these variables changed following bracing. The ACL-deficient subjects showed more knee flexion at heel strike and mid-stance which was assumed to be a compensatory reaction to the ligament deficient knee. The FKB significantly reduced ROM in the ACL-deficient subjects at all gait activity levels (p< 0.05). It also reduced peak knee flexion during swing while walking on level ground, but increased maximum knee flexion in swing while walking on the treadmill. Walking on the treadmill reduced hip ROM but running on the treadmill increased ankle ROM in both groups of subjects. No significant angulatory kinematic changes were found during running on the treadmill either before or after bracing. The ACL-deficient subjects showed more knee rotation than the controls during all the trials. Neither the quadriceps nor hamstring muscles showed significant differences between the ACL-deficient and control subjects. The gastrocnemius muscle however was found to have a principal role in the ACL-deficient subjects. FKBs caused the gastrocnemius to be activated earlier (P=0.0001) and showed a positive effect during low force activities. As treadmill walking or running was always accompanied by an increased ankle plantar flexion, it always decreased the gastrocnemius onset activation time that may be a compensatory reaction to stabilise the injured knee. No significant differences were found between the ACL-deficient and the control subjects in terms of kinematics or EMG findings during running on the treadmill.
We have identified beneficial biomechanical changes following the use of FKBs on ACL-deficient knees but only during walking trials. The brace was as effective for walking on the treadmill as walking on the ground. The FKBs led the deficient knees into a safer kinematics and EMG pattern. The ACL-deficient subjects ran as normally as the control subjects and no effects of the FKBs were found during running in our studies.
The aim of this study was to determine the function of the meniscofemoral ligament in the cranio-caudal and rotatory laxity of the ovine stifle.
Twenty fresh cadaveric ovine stifles were harvested from fully mature sheep, average weight 25kg. The joint was denuded of its muscular attachments leaving the capsule, including the patella and patellar tendon undisturbed. The femur and tibia were divided 10 cm from the joint line, positioned in cylindrical pots, and secured in polymethylmethacrylate bone cement. The stifles were tested in a four-degree-of-freedom rig positioned in an Instron materials testing machine. This allowed unconstrained coupled tibial rotations and translations during application of cranial (anterior) and caudal (posterior) draw forces. Forces up to a maximum of 100Nm were applied in the anterior and posterior directions, and the resultant translations were measured. These parameters were assessed at 30, 60, 90, and 110 degrees of flexion in ten intact stifles. Similar measurements were carried out after division of the caudal (posterior) cruciate ligament, followed by division of the meniscofemoral ligament. The sequence of division was reversed for a further ten stifles.
Division of the meniscofemoral ligament resulted in an 18–38% increase in posterior translation at all angles of flexion, both in the intact and in the caudal cruciate ligament-deficient stifle (p< 0.05). There was no significant increase in anterior translation. This effect was largest with the joint relatively extended (at 30°). Division of the meniscofemoral ligament also resulted in a 5–32% increase in internal rotation of the tibia after application of a 6Nm torque in the caudal cruciate-deficient knee. This was significant at 30° and 110° flexion (p< 0.05).
The meniscofemoral ligament is a significant secondary restraint in resisting the posterior draw and internal tibial rotation in the sheep stifle joint. This is the first study demonstrating a functional role for this structure in any animal. Its counterpart in the human is the posterior meniscofemoral ligament of Wrisberg. Several studies have demonstrated similarities between the sheep stifle and the human knee. Confirmation of a similar role for the ligament of Wrisberg in the human knee would have a significant bearing on the prognosis and management of the posterior cruciate ligament injured knee.
Nicotine is a constituent of tobacco smoke and is present in the body fluids of smokers
Bovine nucleus pulposus (NP) intervertebral disc cells were isolated by sequential digestion of caudal spinal disc nuclei with pronase and collagenase and seeded in 2% alginate at 5x106 cells/ml. The constructs were cultured for 21 days in standard culture medium (DMEM + 20% Fetal calf serum) containing free base nicotine (Sigma) at concentrations ranging from 25nM and 300nM, which reflected the normal physiological concentrations found in the serum of smokers. The medium was replaced every 3 days and representative constructs were removed from culture, digested and assayed for DNA, glycosaminoglycan (GAG) and hydroxyproline content at time points 3, 7, 14 and 21 days. Further constructs were processed for standard histology and immunolocalisation of collagen types I, II and chondroitin-6-sulphate.
The results were analysed statistically using an ANOVA test followed by a non-parametric Dunnit’s test. NP cells demonstrated a dose dependent response. At 25nM dose of nicotine there was a significant increase (p< 0.05) in DNA content, GAG and collagen synthesis in the constructs. At 100nM, 200nM and 300nM doses, there was a significant dose dependent decrease (p< 0.05) in all of these parameters compared to controls cultured under nicotine free conditions. In addition, adverse morphological changes were observed on histology, which included reduced cell proliferation, disrupted cell architecture, disintegration of cells and extracellular matrix. Immunohistochemistry showed the production of type I collagen rather than type II collagen as in the controls.
Nicotine has an overall detrimental effect on cultured nucleus pulposus disc cells in vitro. There was significant inhibition of cell proliferation and extracellular matrix synthesis. Nicotine in tobacco smoke may therefore play a role in the aetiology of disc degeneration that leads to back pain in smokers.
Studies comparing the biomechanical properties of different meniscal repair systems are limited, and most have simply investigated load to failure. Meniscal tissue is highly anisotropic, and far weaker under tension in the radial direction. Loading to failure using high radially orientated loads may, therefore, not be the most physiologically relevant in-vitro test for repair of circumferential tears, and determining increases in gapping across repair sites under cyclical loading at lower loads may be of greater importance. This study aimed to determine the load to failure for 4 different meniscal repair techniques, and to assess gapping across repairs under cyclical loading.
Bovine menisci were divided vertically, 5mm from the peripheral edge to simulate a circumferential tear, and then repaired using 1 of 4 techniques: vertical loop sutures using 2-0 PDS, bioabsorbable Meniscal Arrows (Atlantech), T-Fix Suture Bars (Acufex) or Meniscal Fasteners (Mitek). 9 specimens were tested in each group using an Instron 5565 materials testing machine with Merlin control software to determine load to failure. A further 9 specimens in each group were tested by cyclical loading between 5N and 10N at 20mm/min for 25 cycles. Gapping across the repairs under cyclical loading was measured using a digital micrometer and a Differential Voltage Reluctance Transducer.
The peak load to failure values for each repair method did not appear to fit a Gaussian distribution, but were skewed to the left due to some samples failing at lower loads than the main cluster. Results were analysed using the Kruskal-Wallis test, with Dunn’s multiple comparison post test. The results for gapping across the repairs from the cyclical testing all appeared to fit the Gaussian distribution, and these were analysed by Analysis of Variance, with Tukey’s multiple comparison post test. All analysis was performed using Prism (Graph-pad) Software.
The mean loads to failure for each of the repair groups were: Sutures 72.7 N, T-Fix 49.1 N, Fasteners 40.8 N, and Arrows 34.2 N. The load to failure was significantly greater with the Suture group compared to the Arrows (p< 0.01) or the Fasteners (p< 0.05). The mean gapping across the repairs for each of the repair groups after 25 loading cycles were: Sutures 3.29mm, Arrows 2.18mm,Fasteners 3.99mm,andT-Fix 3.47mm.The mean gapping was significantly less for the Arrows compared to the Sutures (p< 0.05), the Fasteners (p< 0.01), or the T-Fix (p< 0.05).
The results confirm that meniscal repair by suturing gives the highest load to failure, but show that Arrows give superior hold under lower loads, with the least gapping across repairs under cyclical loading by this testing protocol.
The role of matrix metalloproteinases (MMPs) in the aseptic loosening of hip prostheses is well established. Gelatinase MMPs have been identified in the interface membranes and the pseudosynovial tissues in the hips. Little data are available on gelatinase MMPs and their major regulators, including specific tissue inhibitors of matrix metalloproteinases (TIMPs) in the loosening of shoulder prostheses. The objectives of this study were to determine whether A) gelatinase MMPs and their regulators (MMP14, TIMP-1,-2) are produced by periprosthetic tissues in cases of aseptic loosening of shoulder prostheses, and, B) to identify which cell types, in both interface and synovial tissues, localize the enzymes.
Interface tissues and synovial tissues were obtained during revision surgery for loose shoulder implants. In 9 patients (6-Total Shoulder Replacement, 3-Hemiarthro-plasty (Bipolar), 9 samples of interface tissues and 8 samples of synovial tissues were obtained. Of the interface tissues 2 were from the interface of the bipolar and the unresurfaced glenoid. Formalin-fixed paraffin embedded sections were stained using primary antibodies for MMP2 (Neomarkers), MMP9 (Oncogene Ltd), TIMP1, TIMP2 & MMP14 (Chemicon Ltd). Antigen retrieval required pressure cooker treatment for MMP2 and MMP9 and trypsin for TIMP1. Visualisation used a standard DAB chromagen technique (Envision, Dako Ltd.). Appropriate control sections ensured reproducibility of the staining. The antibodies selected bind to both active and inactive forms of the MMPs.
Both HDPE and metal debris were seen in both the synovial and interface tissues. Transformation of macrophages to giant cells was associated with PE debris, and was not observed with metal debris alone.
The presence of gelatinase MMPs in both interface and synovial tissues in aseptic loosening of shoulder prostheses was demonstrated. Differences between the MMP content of macrophages and giant cells between the tissues was detected, positivity was associated with the presence of metallic and/or HDPE debris. Activation of endothelial MMP2 by both MMP14 and low levels of TIMP2 would support the development of a vascular network.
During the last few years there has been renewed interest in hip resurfacing. The advantages of such prostheses include minimal bone resection and more physiological loading of the proximal femur. The purpose of this study was to investigate the stress distribution to the upper femur following a metal-on-metal hip resurfacing and the influence of a short stem on femoral bone loading.
An accurate and validated finite element (FE) model of the proximal femur was utilised. This was created from CT data of cadaveric femurs. The validation process included weighing, modal analysis, strain gauging and ultrasound material testing of the bone. The maximum elastic modulus in the principal direction was 22.9ÊGPa. The elastic moduli of the cement and implant were 1.8 and 200 GPa respectively. The joint force and 4 muscle loads were applied accordingly and adapted to the specific geometry of the bone. The load case represented the 45% position in the gait cycle, corresponding to toe-off. The hip joint force of 2.2kN, approximately 30° superior to the pole of the implant, was applied as a pressure distribution over a 60° spherical segment, modelling the large contact area of the metal-on-metal articulation. Various scenarios with and without an implant were compared.
The distribution of the von Mises stresses in the normal femur without an implant reflected the distribution of the bone’s mechanical properties: the joint load was transferred from the superior surface of the femoral head, through its centre to the dense cortical bone of the calcar and diaphysis. The presence of the resurfacing prosthesis did not significantly affect the stress distribution in the proximal femur, except for a reduction of stresses in the superior region of the femoral head. Varying the length of the stem and its fixation did not significantly affect this stress distribution. A resurfacing prosthesis without a stem resulted in more normal stresses in the superior region of the femoral head.
Compared to the normal femur without an implant the FE analysis of the resurfacing prosthesis demonstrated stress shielding in the superior region of the femoral head. This stress shielding was reduced when a resurfacing component without a stem was used. This advantage must be weighed against the disadvantage that without a stem it is more difficult to accurately position the implant and achieve a uniform cement mantle.
Dual Energy X-ray absorption (DEXA) has been used to measure bone mineral density (BMD) around total hip prostheses. With the recent increase in the use of metal on metal hip resurfacing, such as the Birmingham Hip Resurfacing (BHR), there has been renewed concern over per prosthetic femoral neck fracture and implant loosening. DEXA quantitatively measures bone mineral density and therefore could predict impending loosening and fracture. To the best of our knowledge, there are no recorded studies assessing BMD around metal-on-metal hip resurfacings such as the BHR. Our intention was to produce a reliable method of measuring bone density around a metal-on-metal hip resurfacing, such as the BHR, prior to a prospective study.
We performed DEXA scans on five patients (7 BHR’s), who had undergone resurfacing with the BHR within the last two years, using the Hologic QDR 45000A scanner. Each BHR was scanned twice on the same day with complete patient repositioning between scans. We analysed the data with the Hologic prosthetic hip (v 8.26a: 3) scan analysis software (operating software 9.80D) by identifying a variable number of same-sized regions of interest (ROI) within the femoral neck. These ROI’s were derived from an inter-trochanteric line and the axis of the BHR stem in the femoral neck. Each of the 14 scans was analysed twice, by three of the authors independently; with at least one week between repeat analysis by the same observer. Statistical analysis was carried out by the local University Department of Statistics.
The variation within the same ROI in a given BHR was 0.00353, whereas the variation between all ROI’s was 1.155. The intraclass-correlation was 0.997 (i.e. the correlation between any two assessments of one ROI) with an overall coefficient of variation of 5%. The variation between the two scans for each BHR and between the three assessors was not significant (p=0.87 and p=0.42 respectively). The mean BMD of the individual ROI’s, between the two assessments of the same scans by the same assessor (i.e. intra-observer variation) was lower on the second assessment by 0.0214gcm−2 (SD=0.0025) representing 0.5% mean density for all ROI’s. This difference was statistically significant (p< 0.001).
This method demonstrates excellent reproducibility of the method. Inter-scan and inter-observer variation was so negligible that a tiny intra-observer variation of 0.5% (of mean bone density) became statistically significant (p< 0.001), despite it making no difference to the overall intraclass-correlation. Statistical advice suggested that this very small difference in mean density (intra-observer) only reached significance due to the highly sensitive measurements and excellent reproducibility.
We have designed and demonstrated a safe, non-invasive and highly reproducible method for scanning BHR implants in vivo using DEXA. We will now use this method to prospectively study our BHR population to detect impending loosening or fracture.
Patient disability and handicap following wrist injuries have been the focus of recent research interest
A prospective assessment of unstable (AO types 23-A2, -A3, -C1 and -C2) fractures of the distal radius treated by closed reduction and percutaneous K-wire fixation followed by cast immobilisation was undertaken. One hundred consecutive observations were made during various follow-up time periods up to one year in a group of twenty-five patients (fifteen female and ten male patients, mean age 43 years – range 18 to 67 years). The clinical parameters tested were the range of wrist dorsiflexion, palmarflexion, pronation and supination (measured using a goniometer) and the mass grip strength (Jamar grip dynamometer) following removal of the plaster cast, expressed as percentage of the affected side relative to the opposite normal side. Additionally, each patient completed the Patient-Rated Wrist Evaluation (PRWE) Score
The results of the statistical analysis (Minitab 12.1) gave the following regression (b) and correlation (r) coefficient values: grip strength (b=0.77, r=0.80), dorsiflexion (b=0.58,r=0.78),pronation (b=0.39,r=0.70),supination (b=0.38, r=0.63), palmarflexion (b=0.32, r=0.62).
The present study shows that grip strength (expressed as percentage that of the unaffected side) is the most reliable index of wrist disability and the most sensitive indicator of return of wrist function, followed by the range of wrist dorsiflexion and pronation. Wrist supination and palmarflexion are the clinical outcome variables showing the weakest correlation with the wrist function as rated by the patients. These observations may facilitate correct interpretation and comparisons of the results of clinical studies on various methods of treatment of wrist trauma.
Aseptic loosening is generally associated with the presence of wear particle-associated macrophages in the pseudomembrane commonly formed around failed prosthetic implants. The extent of the macrophage response evoked by the wear particles has been shown to correlate with the amount of periprosthetic osteolysis. Numerous studies have shown that wear particle-associated macrophages contribute to osteolysis by (i) releasing inflammatory cytokines and/or (ii) differentiating into bone resorbing osteoclasts. Although macrophages and macrophage polykaryons are the main inflammatory cells found in periprosthetic tissues, numerous fibroblasts are also present in the connective tissue pseudomembrane. The recently identified molecule, RANKL has been shown to play a central role in the osteoclast formation and bone resorption observed in aseptic loosening. We have shown that arthroplasty macrophages, which express RANK, the receptor for RANKL, are capable of osteoclast differentiation; this process is inhibited by osteoprotegerin (OPG), the soluble decoy receptor for RANKL. As fibroblasts are known to express RANKL, the aim of the present study was to determine whether fibroblasts isolated from periprosthetic tissues could induce the generation of bone resorbing osteoclasts that would contribute to the osteolysis commonly seen in the periprosthetic loosening.
Fibroblast-like cells were isolated from pseudomembrane from patients (n=5) undergoing hip revision due to aseptic loosening, by routine collagenase enzyme digestion. The isolated cells were seeded in flasks for 2–4 weeks before being passaged for a further 3–4 times. Generated fibroblast-like cells (104) were then co-cultured with 5x105 normal human peripheral blood monocytes (n=5) on glass coverslips and dentine slices in the presence of (i) no added factors, (ii) macrophage colony stimulating factor (M-CSF) and (iii) M-CSF plus OPG. All cultures were maintained for 1,17 and 21 days. The extent of osteoclast differentiation was then determined by the expression of specific osteoclast markers including tartrate-resistant acid phosphatase (TRAP) and vitronectin receptor (VNR) and evidence of lacunar resorption.
In the absence M-CSF, no osteoclast formation was noted in 24 hours, 17 or 21 days in fibroblast/monocyte cultures. However, in the presence of M-CSF alone, large numbers of TRAP+ and VNR+ multinucleated cells capable of lacunar resorption were noted in these co-cultures. The addition of OPG, which is known to inhibit RANKL-mediated osteoclast formation, significantly reduced the extent of osteoclast formation and lacunar resorption in these co-cultures.
These results indicate that one means whereby peri-prosthetic osteolysis may occur is by fibroblasts in the arthroplasty pseudomembrane inducing macrophage-osteoclast differentiation. Fibroblasts express RANKL and interact with arthroplasty macrophages, which express RANK and function as osteoclast precursors. These findings indicate that suppression of osteoclast formation by OPG may be a possible form of therapy for reducing prosthetic loosening.
Aseptic loosening of total joint arthroplasty is characterised by osteolysis that is caused by osteoclasts and macrophages. The mechanism of bone resorption is by acidification, dissolution of hydroxyapatite crystals then proteolysis of the bone collagen matrix. The collagen cross-link molecules are cleaved by osteoclasts exposing the N terminal of the cross-link protein - N Telo-peptides (NTx). This represents a highly specific marker for bone resorption. Previously described bone resorption models include radiolabelled animal bones which require the use of animals and radioactive materials or thin dentine slice resorption pits which are only semi-quantitative and technically difficult to produce. NTx could be a potential osteolysis marker in the laboratory investigation of aseptic loosening with the advantage of being cheaper and easier to perform compared to present established marker and also does not require animals or radioactive materials. The aim of this study was to show that NTx generated during osteolysis by cells extracted from human interface membranes of aseptically loosened hips correlates with the established radiolabelled 45Ca bone resorption model.
Cells from human interface membranes of aseptic loosened hip joints were extracted from the tissue following enzyme digestion. These cells were cultured with dead radiolabelled (45Ca) mice calvaria discs in the presence of 1,25 dihydroxyvitamin D3, hydrocortisone, RANKL and M-CSF. In the control culture no cells were added to the culture system. Calvaria discs used for each experiment comparison were from the same parietal bone. The supernatant culture medium were extracted on day 3, 7, 10 and 14 and assayed for NTx and by scintillation counting. On day 14 the remaining culture medium and cells were assayed by scintillation counting. The remaining bone samples were decalcified and the total remaining 45Ca in the bone was measured.
All results were expressed as the ratio of bone exposed to cells (BC)/bone only (B). Supernatant samples for 45Ca showed a rise in BC/B ratio with time 0.83, 0.88, 0.97 and 1.08 (p= 0.0001). Supernatant samples for NTx also showed a rise with time 1.06, 1.21, 1.41 and 1.40 (p=0.03). In the bottom sampling for 45Ca the mean ratio of BC/B was1.8 (p=0.0001) and the BC/B ratio for the remaining radioactivity in the bone at the end of the culture was 0.81(p=0.0007). There was a strong correlation between 45Ca and NTx (r= 0.9).
The absolute values of 45 Ca dropped initially due to the uptake of calcium by the cells and this explains our previously unsuccessful attempt to use non radioactive calcium as a marker of bone destruction. We believe this is the first time human interface membrane cells have been shown to release NTx during osteolysis in an in vitro model. Replacing 45Ca radiolabelled bone with NTx as a marker represents an important step towards simplifying and reducing the cost of an in vitro model of particle induced osteolysis
Mast cells (MC), the tissue-based effector cells in allergic diseases, have many functions. Within bone tissue, they have been linked with new blood vessel formation and marrow fibrosis and it has been proposed that they are capable of promoting osteoclastic bone resorption. MC numbers are known to increase in a number of osteolytic conditions e.g. osteoporosis, hyperparathyroidism and periodontitis. In fracture callus, too, large numbers of MC are present, especially during the onset of remodelling where it is believed they may be responsible for osteoclast recruitment and/or differentiation. The aim of this study was to look for further evidence of mast cell (MC) involvement in pathological bone resorption. MC activity was assessed in tissue sections of osteolytic conditions including Paget’s disease of bone, rheumatoid arthritis and fibrous dysplasia together with several benign and malignant bone tumours. MCs were identified by toluidine blue staining and by immunostaining with a commercial antibody against MC tryptase.
Extensive infiltration of mast cells was observed in fibrous dysplasia, rheumatoid arthritis and Paget’s disease of bone and mast cell accumulation was seen at the bone resorbing margin of a number of enlarging bone tumours including osteosarcoma, giant cell tumour of bone, osteoma and osteoid osteoma.
MCs, along with other inflammatory cells, are known to accumulate at the margins of soft tissue tumours where they are thought to promote tumour growth. The current findings are consistent with a similar role for mast cells in the primary bone tumours examined. In each of the conditions studied, an additional role for MC may be that of promoting bone lysis. MC are known to contain numerous factors including TNF-alpha and IL-1, which are potent stimulators of osteoclast formation and activity.
It is concluded that MCs may contribute to the fibrosis, angiogenesis and increased bone resorption seen in certain metabolic bone diseases. MC activity may also be an important factor contributing to the lysis that occurs in numerous other pathological situations including at the margins of aggressive primary bone tumours and skeletal metastases, leading to the expansion of these lesions.
This study examined the effect of surgical approach on the 1year migration of the Exeter stem, using Roentgen Stereophotogrammetric Analysis (RSA). There is evidence that implants with increased early migration, particularly those moving into internal rotation, are likely to have a higher failure rate.
A total of 46 patients awaiting THR were allocated into 2 groups. Both groups underwent an Exeter Total Hip replacement, one through the Posterior Approach (PA), and the other through the Hardinge Approach (HA). RSA was used to assess post-operative stem position and migration at 1 year. Post-operative gait analysis and clinical evaluation was used to assess a subgroup of patients.
There was no difference in the initial stem position of each group within the femoral canal. Significant differences in migration were found for migration of the head distally and posteriorly and for the tip medially. During gait, the legs of the PA group were relatively internally rotated when compared to those of the HA group. Relative to the supporting bone, the PA implants internally rotate and also rotate into valgus further than the HA implants. The starting position of the prostheses was the same and the cement and prosthesis characteristics were similar. From this, we can infer that surgical approach and therefore muscle function, have a large influence on component migration. During gait, the PA group had internally rotated legs compared to the HA group. This is probably due to short external rotator weakness in the PA group. As a result the internally rotating component of the posteriorly directed joint reaction force on the femoral stem will be larger. This probably explains the rapid internal rotation seen in the implants of the PA group. With the HA group, because of abductor damage there is likely to be a smaller component of the joint reaction force acting on the stem. This would explain the smaller rates of observed coronal plain rotation (rotation into valgus).
Profound differences exist in early migration, between the HA and PA. Different muscle function may account for this and probably influences long-term outcome.
The objective of this study was to examine patients’ use of the Internet to obtain medical information, their opinions on the quality of medical Web sites and their attitudes towards Internet-based consultations.
The study made use of a questionnaire given to 398 patients, aged 10 to 95 years (mean 55 years), visiting the orthopaedic outpatient clinics of a London district general hospital over a 2 week period. The major outcome measures were; 1) the rate of Internet use by patients, 2) the perception of the quality of medical websites, 3) future intentions and attitudes towards internet-based consultations, and 4) concurrence between information obtained from Web sites and advice given by the orthopaedic surgeon in the clinic. Results were considered significant at p< 0.05. The Chi2 test was used to compare proportions. Spearman’s correlation coefficients were used to quantify correlation.
From 369 respondents (response rate 91%), 55.3% of patients had accessed the Internet. Of these 52.0% had obtained medical information from this source. Access was linearly correlated with age (r2 =0.975, p< 0.01) and was also related to social status. Of the 12.3% of patients who had researched their particular orthopaedic condition, 20% reported that the advice received from the surgeon in the clinical contradicted that obtained from the Internet. A total of 37.5% of patients would undergo an Internet-based consultation, whilst a further 25.5% would consider this, depending on the medical condition in question.
This is the first detailed UK study examining patient attitude towards Web-based medical learning. Over half of the patients were willing to access the Internet for medical information, with younger patients more likely to undertake this activity. As the commercial advantages of a captive patient population become apparent, there is the potential for inaccurate or misleading information, that has not undergone peer review, to be disseminated over the Internet The increased use of medical Websites by patients raised important issues regarding the need for quality control, which orthopaedic surgeons and their institutions both need to address. This also impacts significantly upon the changing nature of the surgeon-patient relationship.
Dupuytren’s contracture is characterised by abnormal fibroblast proliferation and extracellular matrix deposition in the palmar fascia. Fibroblast proliferation and matrix deposition in connective tissues are regulated by cytokines. A number of cytokines including transforming growth factor beta (TGFβ), basic fibroblast growth factor (bFGF), platelet derived growth factor (PDGF) and epidermal growth factor (EGF) are known to have potent anabolic effects on connective tissue. The aim of this study was to investigate the role played by anabolic cytokines in the pathogenesis of Dupuytren’s disease.
Twelve specimens of Dupuytren’s contracture and six control specimens of palmar fascia obtained from patients undergoing carpal tunnel release were cultured using a serumless method under standard conditions for 72 h. Levels of TGFβ-1, bFGF, PDGF and EGF in the medium were estimated using an enzyme linked immunoabsorbent assay technique.
Neither Dupuytren’s tissue nor control palmar fascia produced any EGF. The mean (±S.D.)levels of bFGF, PDGF and TGFβ-1 produced by cultured palmar fascia were: 1270 ± 832, 74 ± 24, < 7, and for Dupuytren’s tissue were 722 ± 237, 139 ± 76.6, 645 ± 332, respectively. The levels of PDGF and TGFβ-1 were significantly higher in Dupuytren’s tissue.
PDGF is produced in increased amounts by Dupuytren’s tissue. This may contribute to the fibroblast proliferation and increased ECM deposition observed in this condition. TGFβ-1 is not produced by normal palmar fascia but is produced in large amounts by Dupuytren’s tissue. The major physiologic role of TGFβ-1 is to stimulate formation of fibrous tissue. It plays a major role in wound healing and also in pathological conditions where fibrosis is a prominent feature. Inappropriate production of TGFβ-1 in the palmar fascia in Dupuytren’s disease may play a central role in initiating and stimulating the abnormal fibroblast proliferation and collagen synthesis seen in this condition.
The detection and treatment of acute compartment syndrome following trauma is critical if contractures, delayed fracture healing and possible amputations are to be avoided. The current standard for monitoring relies on invasive compartment pressure measurements. These require an additional procedure and cause discomfort to the patient. This prospective clinical study investigates the relationship between the intra-compartmental pressure and soft tissue oxygenation (%StO2) measured non-invasively by near-infrared spectroscopy (NIRS) in patients at risk of acute compartment syndrome.
Adults with acute tibial or radial diaphyseal fractures were recruited on admission to the orthopaedic trauma unit. Non-invasive and invasive monitoring over anterior tibial or volar forearm compartments was carried out from admission and continued post-operatively. The differential pressure (ΔDP) was calculated as the compartment pressure subtracted from the diastolic blood pressure. The threshold for fasciotomy was a ΔDP < 30mmHg. StO2 values were simultaneously recorded from the contralateral (uninjured) limb at the same site. All patients had the difference between the StO2 value on the injured and uninjured sides calculated (‘StO2 difference’).
Sixty patients with tibial fractures and 5 patients with forearm fractures were recruited. The mean age was 39 years (S.D.18 years). Fourteen patients underwent a four-compartment lower leg fasciotomy determined by a ΔDP < 30mmHg.
We have observed that the difference in StO2 between limbs (measured non-invasively) was significantly lower in patients undergoing a fasciotomy. This suggests that NIRS is able to detect a change in oxygenation of the soft tissues in trauma patients developing an acute compartment syndrome. We are optimistic that near-infrared spectroscopy (NIRS) will be a reliable new non-invasive technique for detection of an acute compartment syndrome.
This study aimed to A) establish a protocol for measuring periprosthetic bone mineral density (BMD) of the proximal humerus following implant arthroplasty, and B) compare the differences in the periprosthetic BMD values 4–9 years after surface replacement and stemmed arthroplasties of the proximal humerus. The study design was of retrospective independent samples cohorts, of patients who had received a proximal humeral arthroplasty between January 1992 and December 1996 in a tertiary referral shoulder unit of a UK hospital. The exclusion criteria were A) patient unavailable for study, B) patient refusal, C) inadequate information of dependent and independent variables, or D) obvious measurement errors.
All available patients underwent DEXA scanning of the proximal humerus using a Lunar DPXL scanner fitted with Orthopaedic Hip software version 1.3. Replicable patient positioning with a special jig was used. On a predetermined format of Gruen equivalent zones and sub-zones, BMD values in gm/cm2 were plotted. Cortical thickness on plain radiographs was recorded for each zone. Femoral neck DEXA scan was performed to obtain a proportionate value of BMD of the proximal humerus, in order to eliminate the effect of confounding variables. Confounding variables accounted for were age, gender, height, weight, activity level, indication for surgery, duration of implantation, dominance, type of arthroplasty (hemi or total) and use of cemented or uncemented stemmed implants. Statistical analysis was performed using Microsoft excel as well as SPSS software.
Initially, 58 shoulders in 52 patients were recruited. 6 patients declined to participate for ill health, 6 had moved out of the area and 8 did not attend or reply. Of the remaining 31 shoulders in 25 patients, 2 patients had an obviously erroneous DEXA reading. 29 shoulders in 23 patients were finally analysed, which included 10 male and 19 female shoulders. Average age was 67.5 years and average time since surgery was 6 years 2 months. Indications for surgery were RA in 14, OA in 8 and other reasons in 7. Of 29 shoulders, 20 received a total replacement, 9 a hemiarthroplasty.
The inevitable obliquity of the image caused some difficulties in maintaining accuracy and difficulties were observed due to limitation of the software to measure thin cortices and to distinguish between the cement and bone. There was no significant correlation between gross cortical thickness and BMD values, and the average periprosthetic BMD was 0.54 g/cm2. Surface replacement implants were associated with relative preservation of proximal medial cortex and higher BMD values in this region. BMD values were consistently higher at the level of stem tip for the stemmed implants. No such phenomenon was observed for the surface replacement prostheses. Hemiarthroplasty was associated with relatively higher BMD values in the proximal medial cortical region than total arthroplasty.
A high incidence of complications with wound healing in calcaneum fractures treated with open reduction and internal fixation (25 – 33% of cases) has been reported. In one study 80% of those who had wound complications required surgical treatment of these. Two recent studies have shown that the risk factors for wound complications in this injury are single layered closure, high BMI, extended time between injury and surgery, diabetes, open fractures and smoking. In our unit, out of a small sample of 56 patients undergoing calcaneal fracture fixation, all those who developed wound complications were smokers.
Transcutaneous oximetry is a technique that has been used routinely to assess oxygen perfusion in neonates and also sometimes in peripheral vascular disease (PVD). It has seen greater use as a research tool in PVD and orthopaedic surgery, being used to look at oxygenation around wounds to assess different surgical approaches. This study was performed to assess whether a difference in the oxygen perfusion around the ankle joint could be measured in smokers and non-smokers. A transcutaneous oximetry probe was used to assess the tissue oxygen perfusion at the ankle (posterior to lateral malleolus where the incision line would be) and on the chest (just to the side of the sternum). A standardised technique was used for each patient.
Patients were chosen who had no lower limb orthopaedic problem or known PVD. The groups were matched in terms of sex and average age. The data was analysed after logarithmic transformation using a two-tailed Students t-test. The average pO2 chest/foot ratio was higher in the non-smokers than smokers but this was not significant (p=0.704). The average ankle pO2 was higher in the non-smokers and this was shown to be significant (p=0.026).
Although a small sample, these data suggest that tissue oxygenation around the ankle may be significantly lower in smokers. This would help to explain why they are at increased risk of wound healing complications. This work also demonstrates that transcutaneous oximetry can be a useful tool in orthopaedic research. Tissue oxygenation around other joints could also be assessed in relation to position to discover the optimum position for wound healing.
Disuse osteoporosis of the greater tuberosity is a consequence of rotator cuff tear. This is a significant problem as the tendon is implanted into a trough within the greater tuberosity during repair. Failure of the repair is a common complication (up to 50%). We hypothesized that failure in re-implantation is due to deficient bone cell response to mechanical stimulation in the tuberosity. In order to establish whether these cells are capable of responding appropriately to mechanical stimuli, the response of bone cells derived from the tuberosity was compared with that of cells derived from the acromion. This was measured in terms of strain related increases in alkaline phosphatase (ALP) activity, nitric oxide (NO) and prostaglandin (PG) production (which are recognised markers of osteoblast differentiation and their response to mechanical strain).
Primary osteoblasts were cultured from samples of acromion and greater tuberosity taken during routine rotator cuff repair (n=5 pairs). The derived cells were placed under cyclic strain at a physiological magnitude for 10 min at 1Hz using well established controls. Samples of media were analysed for changes in NO and PG production and the cells were reacted for ALP. Cells were stimulated with dexamethasone, ascorbic acid and beta-glycerophosphate (established mediators of osteoblast differentiation) then reacted for ALP.
Preliminary results suggest that cells derived from the acromion exhibit significant increases in cellular NO release and in ALP activity, whereas cells derived from the humeral greater tuberosity fail to exhibit any such increases. In marked contrast cells derived from both sites exhibit increases in ALP activity in response to dexamethasone, ascorbic acid and beta-glycerophosphate treatment.
The results suggest that whilst cells derived from the tuberosity after rotator cuff tear respond appropriately to chemical and hormonal stimuli, they are compromised in their ability to respond to mechanical stimulation. It is tempting to speculate that such relationships are also evident in vivo and that they underpin reimplantation failures.
The growth plates of rapidly growing animals have been studied extensively. Nevertheless, several questions remain unanswered, partly because many events happen simultaneously, especially at the vascular front. Terminal chondrocytes are thought to undergo programmed cell death, but the fate of the cell remnants remains unclear. Are the dying cells released into the vascular space and phagocytosed by macrophages, as one would expect for apoptosis? Or are the cells eliminated prior to opening of the lacunae, leaving empty lacunae? Do all terminal chondrocytes die or do some become bone-forming cells? Rodents maintain a growth plate into old age, long after longitudinal growth has ceased. These stationary growth plates have several features not found in the growth plates of rapidly growing animals and closer study of these features may provide answers to the above questions. Femurs and tibiae from 4–16 week-old and 62–80 week-old rats were decalcified, processed into paraffin, and the morphological changes were documented.
Between 4–16 weeks, the heights of the growth plates decreased due to loss of the large hypertrophic chondrocytes, but the various zones were still present. In the aged rats, the growth plates were identifiable as a narrow cartilaginous band with some short columns of inactive cells. The vascular front was irregular, the narrow spicules of primary spongiosa were absent and the much thicker spicules, which are normally seen in secondary spongiosa, directly abutted to the cartilage. Horizontal apposition of bone matrix onto the cartilage edge was frequently present. In addition, the following features were noted. 1) Acellular areas: Nearly all growth plates contained regions of cartilage from which all cells and their lacunae had disappeared. In some cases, these acellular regions stretched from the reserve zone to the vascular front and even persisted as a relatively wide core within the spicules of spongiosa, indicating increased resistance of acellular cartilage to resorption. The absence of cells or cell debris was consistent with an autophagic mode of cell death and subsequent collapse of the lacunae. 2) Remodelling within the growth plate; in some growth plates, large regions of growth plate cartilage had been resorbed and new bone had been laid down in a pattern similar to the remodelling of cortical bone. This suggested that the normal resistance of cartilage to vascular invasion had been lost locally, but was maintained in adjacent non-remodelled regions. 3) Trans-differentiation of chondrocytes to bone-forming cells; extensive new medullary bone formation was noted in the diaphysis of approximately 30% of the aged rats, suggesting that they had received an (unknown) osteogenic stimulus. In these rats, bone matrix was identifiable inside chondrocytic lacunae, and spreading beyond the confines of the lacunae, thus directly replacing growth plate cartilage with bone matrix.
The results suggest that i) chondrocytes are capable of self-elimination, perhaps by a mechanism similar to the autophagic cell death that occurs during insect metamorphosis; ii) resorption of cartilage and vascular invasion requires the presence of the viable chondrocytes; and iii) chondrocytes have the capacity to transdifferentiate to bone-forming cells, but only do so when receiving an increased osteogenic stimulus.
Osteoporosis has been implicated as one of the causative factors for Colles’ fracture. The current study was designed to establish whether the degree of osteoporosis has any influence on the radiological severity of Colles’ fracture in active elderly peri-menopausal female patients.
Female peri-menopausal patients who sustained a Colles’ fracture were studied. The ultra distal Bone Mineral Density (uBMD) was determined using DXA in the contralateral non-fractured wrists, which were also x-rayed. Anthropometric measurements were recorded, the radiological severity of the fracture was assessed using a computerised image analysis system, which measured the radial angle, height and width on AP view and the dorsal tilt on lateral view. Measurements were carried out on the fractured and the normal wrist. Pearson’s correlations between age, height, weight, BMI, uBMD and fracture measurements were carried out. The Bone Deformity Index (BDI) was defined as the summation of all the differences of the previous parameters between the normal and fractured wrists on the AP view. ANOVA, with bonferroni correction, was used to compare the parameters and the radiological measurements between normal, osteopenic and osteoporotic patients.
Sixty-seven patients were recruited. Those with Barton fractures, previous fractures of the wrist or a previous history of chronic treatment with bone modifying drugs were excluded. Forty eight patients were analysed. The parameters measured had a tendency to be worse with increasing degree of osteoporosis, although the only significance was in the measurement of dorsal tilt on the lateral view (p = 0.05). The normal patients were significantly heavier (89.3 kg) than the other two groups (p =0.03). In the osteoporotic group the correlation between uBMD and the BDI was −0.6, between uBMD and radial height difference was –0.5 and between uBMD and the angle difference in AP was also –0.5. Similar correlations in normal patients were not statistically significant. Power estimates were performed. Because of the relatively large variability within the samples, a sample size of 550 cases will be necessary to reach a power of 80% to detect a pre-defined clinically significant difference of 3 units in the BDI between groups.
The evidence from this study suggests that the initial radiological deformity in osteoporotic patients was greater in those patients with severe degree of osteoporosis. The deformity in normal patients did not have a correlation with the uBMD but these patients were significantly heavier, indicating a different combination of causative factors in these two groups. The precision of the current method of x-ray measurements has enabled a precise definition of the variability within the different groups, resulting in the production of information that was not previously available.
Enzymes that breakdown components of the extracellular matrix (ECM) are of fundamental importance, not only in normal bone physiology but also in pathological processes. For instance the temporal and spatial distribution of proteoglycans is not only critical for the mineralisation of bone but is also believed to be responsible for dictating the local bioavailability of glycosaminoglycan-binding growth factors. A sub-family of the ADAMs (a disintegrin and metalloproteinase) has been identified, that contains thrombospondin-like motifs (ADAMTS), and ADAMTS1, 4 and 5 have recently been shown to cleave the major proteoglycan of cartilage, aggrecan. We propose that ADAMTS family members play a novel role in regulating osteoblast function by determining the distribution of proteoglycan in bone.
RT-PCR and Northern blotting experiments have shown expression of ADAMTS1, 3, 4 and 5 in primary rat osteoblasts and in the osteosarcoma cell lines, MG63, TE85 and SaOS-2. ADAMTS1 transcript levels increased with time in primary rat osteoblasts driven by dexamethasone, beta-glycerophosphate and ascorbic acid phosphate to produce bone-like nodules in vitro. Whereas levels of ADAMTS4 that were initially raised in this culture system then became undetectable as mineralisation proceeded.
Since we are interested in the relationship between the osteoblast and matrix molecules, we plated TE85 cells onto an ECM synthesised by MG63 cells and isolated RNA at 1, 24 and 48 hours. Northern analysis showed a transient upregulation of mRNA for both ADAMTS1 and 5 at 1h that was reduced to control levels at 24 and 48h. Transcripts for ADAMTS1 and 3 were also upregulated in primary rat osteoblasts when seeded on ECM molecules like fibronectin and type I collagen for 48 hours. There was however no change in the expression levels of ADAMTS4 when plated on to any of the substrates at any of the time points tested.
These data suggests that cells of the osteoblast lineage express ADAMTS1, 3, 4 and 5 and that individual transcript levels can be regulated by ECM components. The focalised production of ADAMTS family members in response to matrix-derived and other cues may be an important part of bone formation and may have important implications for the way that cells of the osteoblast lineage interact with implant and other biomaterials.
The overall incidence of cuff tears increases with age, individuals over 80years having a 51% incidence of a tear. Currently, the aetiology of rotator cuff tears remains unclear and successful repair is achieved in only 30% patients. Matrix metalloproteinases (MMPs) have roles in a wide range of physiological processes including placentation and embryogenesis, tissue remodelling and wound healing. However, the ability of MMPs to dissolve extracellular matrix has been linked to a variety of pathological processes including rheumatoid arthritis, osteoarthritis, periodontitis and multiple sclerosis, which involve excessive matrix destruction. Production of gelatinase MMPs by torn rotator cuff has been demonstrated. The objectives of this study were to examine the expression of MMPs and their association with histological changes in full thickness tears of the rotator cuff.
Rotator cuff tissue was obtained from ten patients (age 40–80years) undergoing surgical repair. The size of tear was 1–4.5cm; time from presentation to surgery was 1 month (acute) to between 0.5–4years (chronic). Immunohistochemical staining with commercial monoclonal antibodies to a range of MMPs, endothelial, macrophage and fibroblast markers was performed. Production of gelatinase MMPs was measured by gelatin zymography on tissue culture supernatant. Visualisation used a standard DAB chromagen technique.
In the acute specimens there was an infiltrate of macrophages with little collagen degeneration; the fibro-blasts were MMP1 positive and endothelial cells MMP2 positive. At 12 months post-tear mature collagen, plump fibroblasts and proliferating endothelial cells were identified adjacent to the resection edge. Towards the torn edge areas of lower cellularity, sparse vascularity and collagen degeneration were observed. Vimentin positive, CD68 negative cells within this matrix were rounded with foamy cytoplasm, and intensely positive for MMP1 and MMP2, and positive for MMP-3, -10, -11, -13 and -14. Tissue culture supernatant demonstrated active and latent MMP2 production in all cases.
The prolonged interval between trauma and surgical repair, with potential pharmacological intervention, remedial physiotherapy and disuse immobility, make assessment of the factors contributing to tendon degeneration difficult to determine. Fatty infiltration, dystrophic calcification and patchy collagen degeneration were common. However, clear evidence of cellular activities typical of wound repair were also identified, including fibroblast and endothelial cell proliferation. The most striking finding was the association between areas of poor collagen structure with fibroblasts staining intensely for both MMP1 and MMP2 and positive for other matrix metalloproteinases. The production of MMP1 and MMP2 may contribute to active remodelling of the tendon matrix. Success of repair could be influenced by both the quality of the matrix and the cell types and activities in the tissue at the resection edge.
Clinical use of glucocorticoids engenders deleterious changes in bone fragility and initiates apoptosis in osteoblasts and osteocytes. The pathways leading to corticosteroid-induced death in bone remain unclear. Similarly little is known about the effects of ‘bone sparing’ bisphosphonates on osteocytes in vivo. We investigated the effects of bisphosphonates (BPs) on dexamethasone (Dex)-induced apoptosis in the murine osteocyte cell line, MLO-Y4 and studied the putative pathways involved by intervention with inhibitors of signalling molecules, such as p42/44 MAPK and protein kinase A (PKA). Cells were preincubated with N- & non N-containing BPs and/or inhibitors before insult with Dex or H2O2 for 5 hrs. Apoptotic morphology was revealed by acridine orange staining. Activation of p42/44 was identified using Western blotting and in situ immunocytochemistry in the presence or absence of serum.
Both N- & non N-containing BPs were shown to protect against cell death. The addition of inhibitors of p42/44 and PKA blocked the action of Dex. H2O2-induced apoptosis was not blocked by BPs or by any of the inhibitors. Dex appeared to activate p42/44 only in serum supplemented cultures. These data suggest that glucocorticoid but not oxidant-induced osteocyte apoptosis involves activation of p42/44 and that bisphosphonate engendered cell rescue is brought about by inhibition of these MAPK’s. Studies using truncated BPs that lack anti-resorptive activity, and therefore do not interrupt bone remodelling showed that these BPs were also able to protect osteocytes from glucocorticoid-induced death. The ability of bisphosphonates to influence MAPK activation and cell death in the osteocyte opens up exciting possibilities for pharmaceutical intervention during age and steroid hormone related osteocyte loss.
Mesenchymal stem cells (MSCs) are pluripotential cells present in marrow, which have the ability to differentiate into osteoblasts, chrondrocytes and adipocytes. Potential skeletal tissue engineering uses include healing bone defects, spinal fusion and revision arthoplasty surgery. A means of storing viable mesenchymal stem cells is necessary in order for these cells to be readily available for clinical use. The aim of this study was to determine whether cryopreservation has any effect on the osteogenic potential of human bone marrow derived MSCs.
Five normal iliac crest bone marrow aspirates were obtained following informed consent from patients. Each aspirate was divided into two equal samples. Ficoll-separation was used to isolate the MSCs. The fresh MSCs from one sample were cryopreserved, while the other was cultured as a control population. To assess the osteogenic potential of the MSCs after cryopreservation a sample of cells from each population was cultured with osteogenic supplements and the increase in alkaline phosphatase (ALP) and osteocalcin production was compared.
Cryopreservation was not observed to effect the primary cultures of MSCs, which became confluent after a similar period in culture (12–14 days), forming colonies with recognized MSCs morphology. The expression of ALP and osteocalcin after stimulating the MSCs to differentiate with osteogenic supplements, was not significantly altered by the cryopreservation process (P> 0.05).
In conclusion MSCs obtained from fresh human bone marrow aspirates can be cryopreserved without compromise to their proliferation rate or osteogenic potential, confirming that this is a useful means of storing viable cells for future clinical use.
Programmed cell death (PCD) contributes to the pathogenesis of many diseases including osteoarthritis. The principal method is apoptosis that has a well-defined and very characteristic morphology and biochemistry.
The aim of the present study was examine whether the mechanism of cell death in OA chondrocytes was classical apoptosis.
Rat thymocytes were used as controls since these cells are known to undergo classical apoptosis. Human OA cartilage was obtained from femoral head of patients (50 – 80 years) who were undergoing joint replacement surgery. Pieces of OA samples were processed into paraffin and sections incubated with the following antibodies: M3O, an antibody that recognizes the cleavage of cytokeratin 18 by caspases; annexin V, which recognizes phosphatidylserine “flip-flop” that occurs early in the apoptotic process; bcl-2, a protein whose presence protects apoptosis and c-myc, a transcription factor thought to be associated with apoptosis. To induce apoptosis, some samples were incubated with etoposide and staurosporine.
In sections of thymus we noticed the presence of numerous apoptotic bodies. The number increased when the tissue was treated with etoposide and staurosporine. Some thymocytes were immunopositive for M3O and annexin V, and the number of positive cells increased when treated for 2h with etoposide. Chondrocytes of the articular cartilage showed chromatin condensation and many vacuoles but no fragmentation into apoptotic bodies, even when treated with etoposide or staurosporine. The OA chondrocytes were immunonegative for M3O and annexin-V, even after incubation with etoposide and staurosporine. With respect to c-myc and bcl-2, both non-weight bearing and weight-bearing areas in OA sample showed more positive cells then the thymus. More chondrocytes stained for c-myc in the superficial zone of the articular cartilage in the non-weight bearing, while in the weight-bearing areas it was more in the intermediate zone. On the other hand, there were no differences in the distribution of the cells stained for bcl-2 in the articular cartilage. It is known that some events like the phosphatidylserine flip, caspase activation and apoptotic bodies fragmentation occur quickly during apoptosis, so may be difficult to detect.
The results suggest that some features of classical apoptosis, such as phosphatidylserine flip,caspase activation and apoptotic bodies formation did not take place in OA cartilage. It is known that the molecular machinery for apoptosis is not always present in tissues that are undergoing programmed cell death, which seems to be case for OA chondrocytes.
Aseptic loosening of orthopaedic implants has a major financial impact on the Health Service. The process is thought to be caused by wear particles that are phagocytosed by macrophages and hence stimulate bone resorption via a cytokine response. Previous work suggests that factors inhibiting or enhancing bone resorption act through regulation of the OPG and RANK-L mechanism. The objective of this study was to identify the role of RANK-L and OPG within the cytokine response leading to orthopaedic implant loosening.
Ten samples of cellular membrane obtained during revision arthroplasty surgery were analysed with basic histological staining, immunohistology and polymerase chain reaction (PCR). In vitro studies were also carried out using explanted cancellous bone, to which PMMA particles were added and bone resorbing osteoclastic cells were identified by their Tartrate-Resistant Acid Phosphatase (TRAP) activity.
PCR identified the presence of OPG in all of the periprosthetic samples, with RANK-L shown in 40% of the specimens. Immunoreactivity was shown for CD3, CD68 and RANK-L. In vitro studies confirm that there is an initial burst of inflammatory cytokine activity that then subsequently plateaus.
A balance of RANK-L and OPG regulates bone resorption at the bone/implant interface of implants by stimulating a significant initial inflammatory response which leads to loosening.
Experience has shown that oblique fractures can be slow to heal and this has been attributed to excess shear at the fracture site. We routinely treat fractures with hybrid external fixation. In previous studies, olive wires placed through the fracture site reduced shear and this has improved healing times. When the fracture is oblique in the sagittal plane, anatomical constraints prevent the use of olive wires and a new solution is required.
A sawbone tibia with a distal sagittal plane oblique fracture (70° obliquity) was stabilised with a Sheffield Hybrid Fixator. In a pilot study various methods of fixation were tested and six were chosen for further testing. Since the pull-out strength of threads in the plastic bone was poor, olive wires cut behind the olive were used as a mechanically equivalent model for the push-pull system. Seventy degree steerage pins could not be used so 25° pins were tested instead. Cyclic compressive forces (at 10mm/min) of up to 200N axially and in four off-axis positions were applied using a universal testing machine. Fracture site linear motion in three dimensions was measured using an inter-fragmentary motion device, sampled at 100Hz. A standard frame was tested before and after each adaptation and all six methods were applied sequentially to each model.
The results suggest that: I) Arched wires are effective especially under greater bends, 2) Push-pull wires are effective and provide a minimally disruptive solution, 3) Steerage pins are effective especially at steeper obliquities but this may not always be practical, and 4) Placing a half pin in the distal fragment is beneficial but less effective than the use of 2 transverse half pins acting in a compression system (Hutson technique).
Fractures of the tibia should be reduced as accurately as possible. Fractures opened for internal fixation can be reduced accurately under direct vision, but unstable closed fractures treated by external fixation must be reduced by indirect means. Most surgeons reduce the fracture by manipulation, insert the bone-screws, apply the fixator and then manipulate the fracture again to improve the reduction before locking the fixator. Using this technique it is difficult to obtain a perfect reduction. A poor reduction can prolong healing time and may lead to malunion causing long-term impairment of function. A good reduction lessens the loading imposed on the bone-screws and fixator. We describe a device with which closed tibial fractures can be reduced with a predictable high degree of precision prior to external fixation.
A reduction device, the Staffordshire Orthopaedic Reduction Machine (STORM), was developed. Externally fixed unstable closed tibial fractures reduced by conventional methods (n=37) were compared with those reduced using the STORM (n=41). In the STORM group, the holes for the fixator pins were only drilled once the fracture had been perfectly reduced and no further manipulation was undertaken after the fixator had been applied. Reductions were assessed by measurements of radiographs taken at, and 4 weeks after, fixator removal. All cases were treated with monolateral external fixation.
The STORM significantly improves the precision of reduction of unstable tibial fractures without increasing operating time. Its use obviates the need for reduction joints on external fixators for the tibia.
Previous studies in animal models of limb lengthening have shown a wide spectrum of histopathological changes during distraction phase. Much less is known about the structural response of muscle during the consolidation phase. This study aimed to observe and score changes in morphology, weight, length and maximal perimeter of gastrocnemius during the distraction and consolidation phases.
Thirty two immature New Zealand white rabbits were divided into two equal groups: lengthening and sham. In each group, half of the rabbits were killed at the end of lengthening and half 5 weeks later. A bilateral external fixator was applied to tibia and a mid-diaphysis osteotomy performed. The lengthening rate was 0.4 mm twice daily with an initial delay of 7 days. 30% lengthening was achieved in 4 to 5 weeks. After sacrifice, the whole gastrocnemius was taken from its attachments. Its weight, length and maximal perimeter were measured. At the middle of belly, a specimen 0.5cm in length was taken from the medial gastrocnemius for H& E and Masson trichrome staining. A scoring system was used to achieve a semi-quantitative analysis of the histopathological changes in gastrocnemius.
No abnormal changes were observed in the sham side. Degeneration, atrophy and endomysial fibrosis were all found in the lengthened side. The scores of histopathological changes between the end of lengthening and 5 weeks later showed a decreasing trend, but no significant difference. The weight and perimeter decreased and length increased in the lengthening side. The weight, perimeter and length of gastrocnemius in both lengthening and control sides increased at 5 weeks after the end of lengthening.
Muscular atrophy, as shown by a decrease in weight, perimeter and muscle fibre size, occurred and might be due to the combined effect of continuous muscle stretching and inactivity. Continuous stretching of muscles beyond a certain point produced damage. Some studies reported that damage to muscle fibres, which has been shown as degeneration and fibrosis in this study, can release and activate satellite cells. As myoblast precursors, satellite cells become myoblasts, which proliferate and fuse into the microlesioned areas, regenerating and repairing myofibrils. Also, the immature muscles have more active abilities of proliferation, regeneration, growth and healing. In this study gastrocnemius growth shown by an increase in weight, perimeter and length occurred during the consolidation phase of 5 weeks. The mean scores of histopathological changes in gastrocnemius decreased during consolidation period, indicating some recovery of damage to muscle. It is not clear whether this reflects a normal response, which would have been seen in other studies had samples been taken later or whether it is a unique response of the immature animal.
The aim of this study was to establish the ability of an invasive fibre-optic probe to measure intra-muscular pH, pCO2, pO2, HCO3-−, ambient temperature, base excess and O2 saturation. The secondary aim was to determine the effect of elevation of the limb on these parameters.
Fibre-optic probes were introduced into the anterior compartment muscle of the leg in five volunteers via 16G cannulae. After equilibration the limb was monitored for 11min with the volunteer supine on an examination couch. The limb was elevated to 22cm (Braun frame) and then 44cm for the same time. Subsequently the leg was returned to 22cm and supine. All volunteers followed this set protocol. Continuous recording of all indices was made throughout. Data was stored to a personal computer for analysis.
Similar trends were observed across all subjects for all parameters. The mean pO2 when lying flat was 27mmHg (S.D.7.4). Elevation to 22cm increased muscle pO2 to 33 mmHg (S.D. 5.8). Further elevation to 44 cm resulted in a reduction in muscle pO2 to a level below that measured when supine. When the limb was returned to 22cm the pO2 trend reversed, the level improving. Returning to the supine position the pO2 returned to the level seen at the start of monitoring.
This novel probe gives reproducible measures of pH, pCO2, pO2, HCO3−, ambient temperature, base excess and O2 saturation. Results indicate that elevation to 22cm improves muscle oxygenation; a height of 44cm seems detrimental. This technique may be applicable in surveillance for compartment syndromes and muscle ischaemia.
Fracture bending stiffness of 15 Nm/° measured in the sagittal plane provides an objective end-point for healing in tibial fractures treated with external fixation (
A series of omniplanar fracture stiffness measurements were undertaken on patients with tibial fractures treated by external fixation. The first measurements were performed when the fracture was deemed sufficiently stiff to allow the fixator to be removed safely. These were continued at regular intervals until union, defined as a uniplanar stiffness of greater than 15Nm/° in at least two planes.
Polar stiffness plots were obtained and analysed. The stiffness envelope varied significantly in all planes but the general shape of the polar plot remained the same with successive tests, with an overall increase in stiffness. The polar stiffness measurements were significantly different than concurrent uniplanar measurements; this reflects the difficulty in defining the plane of bending accurately in uniplanar measurements. The fracture configuration and healing fibula had unpredictable effects on the polar stiffness.
The measurement of polar fracture stiffness polar gives new insight into how the mechanical environment of a fracture changes during healing. Fracture stiffness is not uniform and this may have implications on when it is safe to remove the fixator.
Current design guidelines for the front end of motor vehicles aim to reduce tibial fractures but this may be at the expense of an increased risk of injury to the knee itself . The purpose of this study was to describe the type of knee injuries and group characteristics of those sustaining them with a view to initiating a more detailed research project in injuries to the lower limb.
The medical records of all patients aged 16 years and over presenting to the Accident & Emergency (A& E) Department at University Hospital Nottingham with a knee injury sustained in a road traffic accident between April 1992 and December 1998 were identified and reviewed.
In a total of 374 patients, 178 sustained significant knee injuries, requiring admission to hospital. 78% of these sustained a fracture, with fracture of the tibial plateau being most common. 22% of patients sustained ligamentous injury. Almost 50% of patients received operative treatment during the first month after injury.
Current legislation may be responsible for placing pedestrians at more risk from knee injuries. An understanding of the mechanism of knee injury compared with tibial fracture is important and recommendations for prevention of injury can then be instituted.
Cementation is an important part of arthroplasty operations. Recent publication of results of Charnley total hip replacement found a rate of early aseptic loosening of 2.3% at 5 years following surgery across a NHS region. There are possibly many reasons for early loosening but precise reasons are still not fully understood, however, it is felt that cementation technique is very important. There seems to be a number of factors involved such as cement mixing techniques and conditions, physical properties of the cement, cementation and surgical techniques, bone-cement interface as well as bone- prosthesis interface. The purpose of this study was to evaluate the effectiveness of the clinical environment in producing bone cement of predictable mechanical and physical properties, and how those properties compare with published data. The investigation compared samples of bone cement, taken from material prepared and used in surgery with cement samples prepared under controlled laboratory conditions and in accordance with ISO materials testing standards.
During 2000–01, 10 total hip replacements were selected for study. All operations involved the use of CMW1 (DePuy) radio-opaque cement, which was mixed using the Vacumix system. In this cohort, all femoral cementations were performed using an 80g cement mix. After careful preparation of the femoral canal, the scrub nurse mixed the cement in accordance with the manufacturer’s instructions. The cement was introduced into the femoral canal, via a nozzle, using the cementation gun and a pressurizer. Following introduction of cement into the canal, the nozzle and cement contained within, was broken off the gun distal to the pressurizer. Once cured, the cement samples were removed from the nozzle, sectioned, and mechanically tested. Due to this novel sample preparation procedure, the tested cement was expected to exhibit mechanical and physical properties characteristic of the cement present in the femoral canal. Samples of CMW1 (Vacumixed) of similar mass and aspect ratio were produced within the laboratory, in accordance with the manufacturers mixing instructions. PMMA bone cement is a brittle, glassy polymer that is susceptible to stress raisers, such as pores, which can reduce the load carrying ability, which
The surgical samples were found to be very consistent in compressive strength (121 ± 6 MPa), density (1.20 ± 0.02 gcm−3) and hardness (23.2 ± 1.6 VHN) and closely matched the mechanical properties of the cement mixed in the laboratory.
This study suggests that for the studied cement and mixing regime, the clinical environment is capable of producing a well-controlled cement product that has reproducible and predictable mechanical properties. Further, the novel sample preparation procedure used suggests that the cement within the femoral cavity should demonstrate equally predictable, mechanical and physical properties.
A research programme has been directed at the mechanism by which car occupants sustain ankle and hind-foot injuries. The severe injuries that are most associated with long term disability and high socio-economic cost have been investigated. Although seat belts and air bags have had a beneficial effect on injuries to most body regions including pelvic, femur and knee injuries, no protective effect has been demonstrated for below knee injuries. Only by understanding the mechanism of injuries to the leg below the knee will it be possible to design improved protection in the future.
Twenty three post mortem human surrogate (PMHS) limbs were impacted using a test set up that was developed to simulate the loading conditions seen in a frontal collision in 3 different positions – A, B & C. The impactor head (5cm x 10cm wide), was instrumented with an accelerometer and linear potentiometer. The impacting force was generated using a bungee-powered sled mounted on steel bearings. Three PMHS legs were tested In Position A (impactor head centred in line with the tibial axis), 9 PMHS legs were tested in Position B (impactor head centred on the anterior tibial margin) and 11 PMHS legs were tested in Position C (impactor head centred 2.5cm anterior to the anterior tibial margin). Active dorsiflexion was simulated through the Achilles tendon and prior to the application of Achilles tension a tibial pre-load (500 to1500N) was applied via a ‘jacking-plate’ applied to the proximal end of the tibia.
During impact testing, bone failure (fractures) occurred at impact loads of 5.7+/−1.9 kN (resultant tibial failure load 6.4+/−1.9 kN) and the following injuries were generated: 9 intra-articular calcaneal fractures; 1 talar neck and 2 talar body fractures; 3 intra-articular distal tibial (pilon) fractures; 2 malleolar fractures; 3 soft tissue injuries and in 3 cases there was no detectable injury. The impact test conditions were replicated with a Hybrid III leg in a first attempt at developing injury risk functions for the dummy.
This study has demonstrated the importance of preload through muscle tension in addition to the intrinsic properties of PMHS specimens in the generation of severe ankle and hindfoot injury.
The purpose of this study was to investigate the influence of ligamentous restraints on first metatarsal (MT1) movements in the context of hallux valgus (HV), the surgical correction of which relies on a sound understanding of factors leading to MT1 deformity. Hypermobility or instability of the first metatarsal at its tarsometatarsal joint (TMJ1) is associated with greater degrees of deformity and also greater risk of recurrence after surgery. Recent anatomical work has shown the importance of the plantar aponeurosis (PA), and the transverse ‘tie-bar’ system (TTB) of the metatarsophalangeal (MPJ) plantar plates and intervening deep transverse inter-metatarsal ligaments in the structure and function of the foot. These ligamentous systems are important in MPJ stability, but may also be important at TMJ1.
Ten normal cadaveric feet were dissected to expose the capsules and ligaments of the MPJs and TMTJs and the PA. They were then mounted in plaster of Paris leaving the MT1, MT2, and their articulations free. A loading fixture was constructed so that loads could be applied to MT1 in the transverse plane to produce moments in flexion, abduction or extension. The movements resulting from a load of 40N were measured relative to MT2 using an Isotrak II (Polhemus, US) magnetic measurement system. The tests were performed with the hallux mobile, fixed neutral and fixed dorsiflexed at the MPJ. After an initial test with all structures intact, the PA and the TTB were severed in random order and the test repeated. “Movement maps” were produced showing the range of motion available in different directions and with different ligamentous restraints.
Movement maps suggest that the TMJ1 behaves as a ball and socket joint with no preferred axis of motion. The contributions of the PA and TTB to stiffness in the sagittal plane are small (about 1° movement). However, the TTB provides significant control of the abduction of MT1. The control afforded by the TTB is particularly important since it can ensure that the PA acts to provide an adduction moment about the TMJ1. The integrity of these ligamentous structures is likely to be important in the success of corrective surgical procedures for HV, where disruption can allow up to 10° increase in MT1-2 angles.
Polymerisation of PMMA results in a volume change resulting from molecular rearrangement. The calculated maximal volume reduction is approximately 7.6%; however, void growth reduces this to 3–6%. The significance of volume reduction is controversial, in particular with reference to void elimination techniques. Whilst the impact of mixing technique on overall volume change is known, little is understood about the dynamic volumetric changes occurring during the crucial time of cement-bone micro-interlock formation. This study aimed to investigate the volumetric behaviour of bone cement during polymerisation.
Polyethylene tubes were modified to simulate the physical and dimensional constraints of the human femoral medullary canal. The tubes were filled with either hand or enhanced vacuum mixed cement and suspended in a water bath. The residual weight of the cement specimen in water was recorded at 60sec intervals for 30 minutes. The dry weight of the cement is known and the immersed weight can be calculated. Archimedes principal allows calculation of the density and thus the volume of the cement mass throughout polymerisation. The specimens were sectioned, stained and analysed to assess sectional porosity.
In no specimen was it possible to demonstrate overall net expansion, however, hand mixed specimens demonstrated a temporary period of expansion during the early exothermic period. Vacuum mixed specimens demonstrated progressive contraction only. Overall volume change correlated closely with sectional porosity.
The overall volume reduction is strongly influenced by porosity. The temporary expansion observed in porous cement specimens must result from temperature driven growth of voids. This expansion occurs during the crucial period of cement-bone micro-interlock formation, and may therefore enhance attempts at pressurisation. Conversely, progressive volume reduction, as seen with low porosity cement, may impede micro-interlock formation. Successful cementation using vacuum mixed cement may therefore be solely dependent on adequate cement pressurisation.
The restoration of pain-free stable function in gleno-humeral arthritic cases in various situations such as rotator cuff deficiency, old trauma and failed total shoulder arthroplasty is a challenging clinical dilemma. The Bayley-Walker shoulder has been designed specifically for very difficult cases where surface replacement devices do not provide sufficient stability. This device is a fixed-fulcrum reversed anatomy prosthesis consisting of a titanium glenoid component with a CoCrMo alloy head that articulates with an UHMWPE liner encased in a titanium alloy humeral component that has a long tapered grooved stem. The centre of rotation of the Bayley-Walker shoulder is placed medially and distally with respect to the normal shoulder in order to improve the efficiency of the abductor muscles. An important problem in devices of this type is obtaining secure and long-lasting fixation of the glenoid component. The glenoid component relies on fixation through the cortical bone by using threads, which protrude through the anterior surface of the scapula at the vault of the glenoid. It is HA coated for subsequent osseointegration. The purpose of this study was to investigate fixation of the glenoid component.
A 3D finite element model of the glenoid component implanted in a scapula was analysed using Abaqus. The implant was placed in position in the scapula, with the final 2–3 screw threads cutting through the cortical bone on the anterior side at the vault of the glenoid due to the anatomy in this region. The analysis was performed for two load cases at 60° and 90° abduction. A histological study of a retrieval case, obtained 121 days after implantation, was also conducted.
The FEA results showed that most of the forces were transmitted from the component to the cortical bone of the scapula, the remaining load being transmitted through cancellous bone. In particular the area where the threads of the glenoid component penetrated the scapula showed high strain energy densities. Histology from the retrieved case showed evidence of bone remodelling whereby new bone growth resulting in cortical remodelling had occurred around the threads.
Both the FEA and histological study show that fixing the component at multiple locations in cortical bone may overcome the problems of glenoid loosening associated with constrained devices. The Bayley-Walker device has been used on a custom basis since 1994; 81 Bayley–Walker shoulders for non-tumour conditions and 43 Bayley-Walker glenoid components have been used in association with a bone tumour implant, with good early results. Radiographically, radiolucencies have not been observed and overall the comparisons with the original Kessel design are positive.
It is generally appreciated that the internal structure and external shape of living bone adapt to mechanical stimuli according to Wolff’s law. However, the precise details of bone adaptation to external forces are not fully understood and there has been no previous investigation of the association between specific loading conditions and the skeletal architecture of a particular anatomical area using case-specific observations in a group of individuals. The aim of the present study was to investigate a previously unreported correlation between the maximum wrist joint reaction force and the volar tilt angle of the distal radius using parameters radiographically obtained parameters from normal wrist joints.
Using free body analysis of the forces acting on the distal radius for the loading condition that corresponds to the lift of a weight using the supinated hand, the wrist joint reaction force F and the angle formed between the vector of F and the long axis of the radius have been expressed as a function of the lifted weight, the lever-arm of the wrist flexor tendons and that of the lifted weight. Measurements of the volar tilt angle of distal radius and the lever-arms of the flexor tendons and the lifted weight were performed from lateral wrist radiographs of 30 normal wrists. Subsequently, using the equations obtained from free body analysis, the maximum wrist joint reaction force F and the angle that the latter forms with the long axis of the radius were calculated for each the cases. Statistical analysis compared the angle of the maximum wrist force and the volar tilt of the distal radius (two-tailed paired t-test) and correlated (a) the angle of the maximum wrist force and the volar tilt angle and (b) the maximum joint reaction force and the volar tilt angle.
Results showed no significant difference (p=0.33, 95% confidence interval −0.64° to 0.22°) but a statistically significant correlation (R2 = 0.74, r = 0.86, p < 0.001) between the angle of the maximum wrist force and the volar tilt angle of the distal radius. Additionally, an inverse relationship between the volar tilt angle and the magnitude of the maximum wrist force (R2 = 0.71, r =−0.84, p< 0.001) was found.
These observations may explain the mechanism of the phylogenetical development of the volar tilt angle and support the ‘minimum effective strain’ theory of adaptive bone remodeling
Clinical implantation represents the ultimate experiment of any component and often demonstrates areas of strengths and weaknesses not predicted from in vitro testing. Mobile bearing knees incorporate an additional articulating interface between the flat distal PE insert and a highly polished metal tibial tray. This can allow the proximal interface to retain high conformity whilst leading to reduced stresses at the bone – prosthesis interface by permitting complex distal interface compensatory motion to occur (rotation and/or translation). Retrieval reports on many of the new generation of mobile bearing implants remains scarce. This study presented a retrieval analysis of 9 mobile bearing inserts that had be in situ for less than 24 months.
Nine cemented mobile bearing implants (6 AP Glide, 1 LCS, 1 MBK and 1TRAK) were received into our Implant Retrieval Program. The femoral component, tibial tray and PE insert were macroscopically examined under a stereo-zoom microscope for evidence of damage. The PE inserts were graded for wear based on optical and SEM assessments. The proximal and distal surfaces of the PE inserts were subsequently assessed for surface roughness following ISO 97 (Ra and Rp) using a Surfanalyzer 5400 (Federal Products, Providence, RI). Virgin, unused PE inserts were analysed and served as a comparison to the retrieved implants.
Time in situ time for these implants ranged from 6 months to 24 months (mean 18.6). The implants were revised for instability and pain (AP glide) or dislocation (TRAK). Damage to the femoral components, in general, was minimal with some evidence of a transfer film of PE. The proximal surface of the tibial trays presented evidence of PE transfer as well as some scratches but in general were intact. The proximal PE and distal PE articulating surfaces demonstrated significant areas of damage due to third body wear which was identified on EDAX to be PMMA. Areas of burnishing were also present at the proximal and distal interface. The damage, in part, correlated with the complex kinematics of each design.
Metacarpophalangeal (MCP) arthroplasty usually involves the fitting of a silicone spacer, commonly Swanson prosthesis, but more recently the Sutter prosthesis has been introduced.
Four Sutter MCP prostheses, two each sized 30 and 40, were removed from the right hand of a female patient. The patient aged 61 years ate revision, had longstanding rheumatoid arthritis. Using a single station finger stimulator
These are the first reported in vitro results of fracture of Sutter prosthesis as well as the first paper to state the site of ex vivo fractures of Sutter prostheses. A computer model described in a recent paper
Infection around implanted biomaterials in humans is a major healthcare issue and current ability to effectively prevent and treat such infections using antibiotics is limited. The hypothesis of the study was that surface charge could be manipulated to a positive state and thus moderate bacterial adhesion to the implant. The surface charge was manipulated by creating a galvanic cell using a zinc strip in a standard suction drain.
Adhesion of
In this experiment we have shown that alteration of the electrochemical environment around an implant influences bacterial adhesion. While our technique is not therapeutically viable, further manipulation of surface charge of an implant is possible using other electroactive materials. This may be explored in the prophylactic treatment of implant infection
There has been speculation as to whether the outcome of revision total knee arthroplasty (TKA) is as successful as primary TKA. The purpose of this study was to assess patient outcomes following revision TKA and compare them to patient outcomes following primary TKA.
This study collected data prospectively from patients operated upon by one surgeon using one prosthesis in each group. Patients completed SF12 and WOMAC questionnaires pre-operatively and at six and twelve months post-operatively. In the primary TKA group there were 84 patients. In the revision TKA group there were 60 patients. Statistical analysis was performed using paired and unpaired t-tests.
Results showed that the improvements in SF12 physical scores and WOMAC pain, stiffness and function scores in both primary TKA and revision TKA patients were statistically significant (p < 0.0001). There was no significant difference in the magnitude of the improvement in SF12 physical (p = 0.7145) and WOMAC pain (p = 0.0902), stiffness (p = 0.1557) and function (p = 0.3152) scores between the primary and revision patients following surgery.
The mental scores of patients in both groups showed no significant difference following surgery (Primary p = 0.823, Revision p = 0.7095).
The findings show that primary and revision TKA lead to a comparable improvement in patient perceived outcomes of physical health parameters.
However, there is no significant improvement in patient perception of mental health.
Controversy exists as to whether the biomechanical properties of a 360 lumbar fusion are influenced by the order in which the anterior and posterior components of the procedure are performed.
The fusion technique used Magerl screws to effect the posterior fusion and a Syncage implant (Stratec) to effect the anterior component of the fusion.
Isolated motion segments from calf spines were tested in each of two groups of five. In the first group the posterior fusion was performed first and in the second group the anterior fusion was performed first. Loads were applied as a dead weight of 2Nm in each range of movement of the spine (flexion/extension, lateral flexion and rotation). The range of movement was measured using the Qualisys motion analysis software linked to a set of five cameras, using external marker clusters attached to the vertebral bodies. Each motion segment was tested prior to instrumentation, post anterior or posterior instrumentation and with both anterior and posterior instrumentation.
Ranges of movement following 360 instrumentation were increased in all planes tested when posterior fixation was performed first; flexion/extension 26% v 55% (p=0.020), lateral flexion 18% v 34% (p=0.382), and rotation 18% v 73% (p=0.034).
It was concluded that posterior fixation should not be performed prior to anterior fixation as this results in a significant loss of stability in both flexion/extension and rotation
The inhibition of neural input by infiltration of local anaesthetic around the operation site prior to the trauma of an operation may reduce subsequent pain post-operatively. Prevention of the normal phenomenon of central and peripheral sensitisation in the nervous system stops the post operative hypersensitivity state that manifests as a decrease in the pain threshold at the site of injury. The underlying clinical principle is for therapeutic intervention to be made in advance of the pain rather than as a reaction to it
Thirty six patients undergoing day case unilateral knee arthroscopy between October 2000 and March 2001 were studied. All patients gave written informed consent. They were randomised into 2 groups using block randomisation to ensure equal group sizes. The sealed envelope technique was used. The pre-operative group had 10ml 0.25% bupivicaine infiltrated around the arthroscopy portal site following induction of general anaesthesia (G.A.), the post-operative group received 10ml 0.25% bupivicaine after the procedure but before reversal of the G.A. The injection technique and G.A. used were standardised. Pain was assessed using a 10cm Visual Analogue Score (VAS) at pre-operative, 1, 2 and 24h post-operative. At each assessment the patients were blinded to the previous scores that they had submitted. Oral analgesic use in the post-operative 24 hours was also recorded.
There were 18 patients in each group. Demographic details did not differ between the 2 groups. One patient in the post-operative group was excluded, as intravenous sedation was required in recovery due to an extreme anxiety state. The mean Visual Acuity Pain Scores (VAS) were lower in the post-operative group (1.3) compared to the pre-operative group (1.58) at pre-operative assessment. However this difference was not statistically significant (p =0.5607). At 1h post op the mean VAS in the post op group was 1.58 and in the pre op group 2.59 (p =0.18). The mean VAS at 2h post op in the pre op group was 1.76 compared to 1.82 in the post op group (p =0.9932).
At 24h the pre op group had a lower mean VAS (2.25) than the post op group (2.4). This difference was however not statistically significant (p =0.7418).
Analysis of the postoperative analgesia requirement in both groups failed to reveal a statistically significant difference (p =0.3965). In day case knee arthroscopy under general anaesthesia there is no beneficial role in the use of pre-emptive local anaesthetic infiltration around the arthroscopy portal sites as compared to post-operative infiltration.
The use of crude mortality and morbidity data to assess the outcome from surgical intervention can be both dangerous and misleading. Furthermore, differences in outcome when comparing differing units or surgeons may be explained merely by variations in case mix and the type of surgery.
In recent years there have been a number of attempts to devise a reliable method for assessing the outcome from surgical intervention. In the general surgical setting, the POSSUM system has proved to be the most reliable and accurate of all scoring systems so far devised. It is widely applicable in other specialities as it allows comparison based on the patient’s physiological status and the magnitude of surgery. It could be used in any hospital, in elective and emergency operations. The present study attempted to validate the application of this new method of assessing the outcome after orthopaedic surgery.
All consecutive patients admitted to the orthopaedic wards in a district general hospital during a 12 month period in which orthopaedic surgery was performed on a non-day case basis were assessed using the new orthopaedic POSSUM system. POSSUM is an acronym for
During the 12 month period
The present study indicates that orthopaedic POSSUM is accurate in assessing outcome after an orthopaedic operation and can be used as an audit aid to assess the quality of surgical care.
Therapy against Methicillin resistant Staphylococcus aureus (MRSA) infection is mainly restricted to the glycopeptide agents (vancomycin and teicoplanin), which require parenteral administration. At present oral antibiotic therapy against MRSA infection is not available. Linezolid is a recently introduced oxazolidinone synthetic antibiotic which acts by inhibiting the initiation of bacterial protein synthesis. It is effective against MRSA, glycopeptide resistant enterococci and all pneumococci irrespective of their penicillin or macrolide resistance. It has excellent oral bioavailability however, there are no data on the penetration of linezolid into osteoarticular tissues. This aim f this study was to measure the concentration of Linezolid in osteoarticular tissues after oral and intravenous administration.
Ten patients undergoing primary total knee replacements for osteoarthritis or rheumatoid arthritis were included in the study. Linezolid was given orally 600mg BD dose for 2 days prior to operation and a final IV 600mg dose 1h before induction on the day of operation. Intra-operatively at 30min after induction, blood, synovial fluid, synovium, muscle and bone samples were collected, processed and assayed for Linezolid concentration. The assay was performed by High Performance Liquid Chromatography (HPLC) method at Antimicrobial Research Laboratory, Westmead Hospital, Bristol.
High concentrations of Linezolid, above the Minimum Inhibitory Concentration (MIC≤ 4) were obtained all sites. Mean (± SD) concentrations for different tis- were: serum 23.0 (6.5) mg/L, synovial fluid 20.1 .4) mg/L, synovium 18.0 (5.6) mg/kg, muscle 18.5 (6.6) bone 8.5 (3.9) mg/kg
Treatment of Methicillin resistant
12 GPs were invited to take part in a study in which the GPs would undertake training in out-patient techniques, to determine suitability of patients for arthroscopic surgery. The GPs would undertake to counsel the patients regarding the procedure itself and the post operative rehabilitation. They were then referred by means of a set referral form which included specific guidelines which allowed patients to be put directly onto the consultant’s waiting list. The patients would then be sent for surgery directly and be seen immediately pre-operatively by the operating consultant and consented. This group of direct access arthroscopy patients (36) were compared to a contemporaneous consecutive series of patients who had been referred in the normal manner and were undergoing operation at the time of the study period (October 1998 to April 2000.
In the group of patient submitted for direct access arthroscopy three patients had improved such that when they were offered admission dates they declined. A further three patients were deemed unsuitable for direct access arthroscopy and the referral was rejected by the consultant. Two patients declined three separate admission dates and were discharged, and a final patient did not attend his admission date. This left 27 patients who were admitted for direct access arthroscopy service. Of these, one patient was cancelled pre-operatively by the consultant as she had recently been admitted for investigation of cardiac abnormalities procedure and was therefore considered unfit for day case general anaesthetic procedure. Of the 26 patients who underwent arthroscopy all were discharged home the same day, and reviewed in the out-patient clinic at six weeks, and they were asked to complete a Patient Satisfaction Questionnaire, and were discharged from further review at that time.
When compared to a contemporaneous group of patients who had undergone arthroscopic surgery via the routine referral procedure, the group of patients admitted via the direct access route waited on average ten weeks (range 6 – 12) from GP consultation and referral to operation date. This compared to 41 week for the combined total out-patient and in-patient waiting times for the routine access group (range 18 – 132 weeks). Findings at arthroscopy were similar in the two groups with mostly meniscal lesions (18/26 direct access group compared to 15/26 routine access group). The therapeutic operation rate, i.e. procedures beyond simple diagnostic arthroscopy were undertaken, was high in both groups, 68% of the direct access group and 72% of the routine access group. Pre-operative diagnosis accuracy by the GPs was significantly higher in the direct access group of referrals. 65% of direct access referrals had the correct diagnosis made by the GP in the referral compared to 18% of correct diagnosis in the group undergoing routine referrals. Post operative recovery in terms of return to work , return to activities of daily living and discharge from clinic was the same in the two groups. Patient satisfaction was comparable in both groups.
In conclusion direct access arthroscopy reduces significantly the time the surgery and the number of visits by patients to primary or secondary care physicians. GP diagnostic rates were comparable to previously reported figures for registrar/middle grade pre-operative diagnostic rates for patients undergoing knee artrhoscopy. There was a high therapeutic operation rate suggesting few, if any inappropriate procedures were undertaken. The direct access arthroscopy service requires considerable time on the part of the consultant in both setting up the study and training the GPs to a reasonable standard and monitoring referrals and undertaking pre-operative screening of patients awaiting arthroscopy. There was a high inappropriate referral rate in that only 26 patients out of the 36 referred eventually underwent arthroscopic surgery. Although feasible we feel that direct access knee arthroscopy service needs refinement if it is to continue. We intend to introduce an orthopaedic practitioner who will accept referrals from GPs and then screen patients before placing patients on the consultant’s inpatient waiting list. Also the mechanism of extra lists needs to be put in place to ensure direct access patients do not “jump the queue” of patients who are already awaiting arthroscopic surgery.
To clarify the normal range of articular cartilage volumes of the patella and femur in the human knee joints of healthy adults using three-dimensional magnetic resonance imaging and to analyze the correlation of the articular volumes with the background characteristics.
Fifty seven knees of 57 healthy volunteers aged from twenties to forties (30 males and 27 females), who had no past history of joint disease or trauma in the legs, were imaged by a fat-suppressed three-dimensional sequence (SPGR; 1.5T GE; Horizon LX 8.2.5) The obtained data were analyzed by 4 examiners independently with a computer workstation, and a average of the four was adopted as the articular volume. Analyzed characteristics factors of the volunteers were: age, body weight, height, leg length, foot size, circumference of the thigh and lower leg, quadriceps angle, foot angle, body-mass index, and general laxity.
The mean articular cartilage volume was 7.2 +- 1.6 ml. It was significantly larger in males than in females. Concerning the relationship between the volume and the characteristic factors, there was a significant correlation of the cartilage volume with the foot size in males (r=0.47), and with height, leg length and foot size in females (r=0.53, 0.60, 0.60, respectively), but no significant correlation with the other factors.
Conclusion. The articular cartilage volumes of the patella and femur was 7.2+- 1.6 ml. The size of skeletal structure, especially the skeletal size of the lower extremity, were assumed to be important factors in estimating cartilage volume.
Presently, many instruments exist for assessing both patient - and surgeon-based satisfaction after joint replacement, including both generic (measures of general health status) and disease specific measures. As such, the US PORT study (1995) recommends use of both the WOMAC and SF-36. However, this means that studies need to incorporate at least these two lengthy questionnaires into protocols, which increases the pressure on patients for both time and difficulty, but also introduces some duplication of data.
The SF-36 has been successfully reduced and validated to a 12 item questionnaire (SF-12) which can be used as a summarised generic health score. It would be of great benefit if a reduced version of the WOMAC could be derived to give a similar summarised disease-specific measurement tool.
To derive and assess the validity of a reduced function scale of the WOMAC for patients with osteoarthritis of the hip and knee.
All unilateral data from 12 centres world-wide (UK US Canada and Australia) involved in an international, multi-centre outcome study for patients undergoing TKR were included for analysis. The reduced scale was derived from pre-op and 3 month post op data using a combination of data-driven analysis and purely clinical methods. The reduced WOMAC was then extensively validated in three key areas; validity, reliability and responsiveness using 12 month post-op data from the study and data from the Medicare Hip Replacement Study.
Data from 898 patients pre-operatively and 806 patients at 3-months were used for the data driven section of analysis. For the clinical section, 30 members of the orthopaedic community were surveyed as to their opinions of which items should be retained in the reduced version of the scale. These results were then combined to produce a reduced function scale of 7 items to be used in conjunction with the 5-item pain scale. The questions remaining in the scale (and their original number in the scale) were: 2) ascending stairs, 3) rising from sitting, 6) walking on flat, 7) getting in/out of car, 9) putting on socks/stockings, 10) rising from bed and 14) sitting. This reduced scale was then scrutinised to ensure it’s validity (both construct and content), reliability (both internal consistency and reproducibility) and responsiveness (using Standardised Response Means). When examining 12 month data the reduced scale compared favourably with the full scale both overall, and when sub-divided by age, sex and country. It’s construct validity was confirmed by significant positive correlation with the SF-36 physical component score, the knee society function score, the Oxford knee score, and for the hip data, the Harris hip score and SF-12 physical component score. Cronbach’s alpha was consistently high (α> 0.85) with the reduced scale, showing it to be reliable, and the SRM’s indicated that the reduced scale may even be better at detecting change than the full scale.
This reduced WOMAC has been successfully derived and validated for use as a summarised and more practical version of the full WOMAC scale.
It was aimed to investigate the isolated effect of hydrostatic pressure on chondrocyte metabolism. Chondrocytes obtained from bovine metatarso-phalangeal joints were cultured in cylindrical 2% agarose gels. A special apparatus which was designed and constructed, allowed the application of hydrostatic pressure of either 2 MPa or 5 MPa on the chondrocytes for 4 hours either in a pulsatile (1Hz) or a static manner. Changes in the syntheses of glycosaminoglycan (GAG) and DNA during and after the application of the hydrostatic pressure were analysed with 35S-sulphate and 3H-thymidine incorporation, respectively. Radiolabelling was carried out for the following conditions: (a) 4 hours during the application of hydrostatic pressure; (b) 4 hours and (c) 20 hours immediately after the application of load. In addition, the experiments were carried out at 2 days, 7 days and 14 days after embedding the chondrocytes in agarose gels. Static hydrostatic pressure of 5 MPa caused a significant increase by 13% on average in the GAG synthesis during the load application on Day 2 7 and 14 (p < 0.05). On the contrary, pulsatile pressure of 2 MPa caused a significant decrease by 17% in the GAG synthesis measured at 20 hours after the loading on Day 14 (p < 0.01). In addition, there was a significant decrease by 29% in the DNA synthesis measured at 4 hours after the pulsatile loading of 5 MPa on Day 7 (p < 0.01). The results suggest that hydrostatic pressure alone, which causes no cell deformation, can affect the GAG synthesis and proliferation of chondrocytes. In addition, the effect of hydrostatic pressure on the chondrocyte metabolism varies according to the regimes of loading and with the period of cell culture.
The purpose of this study is to evaluate the relationship between the clinical results and the angle of the reconstructed ligament measured radiographically.
We also describe the comparison of the results by the fixation technique of the femoral tunnel. We retrospectively evaluated 90 patients who had arthroscopy assisted ACL reconstruction using middle-third middle-third bone patellar tendon autograft. There were 67 men and 23 women. Their average age at surgery was 23.9 years. The average follow up periods was 28.0 months. We used interference fit screw for grafted ligament fixation of the femoral and tibial tunnel. 71 patients received inside out technique and on 19 patients outside in technique as for the fixation of the femoral funnel.
The lateral angle and A-P angle of the reconstructed ligament were measured roentgenographically. Data from KT-2000 arthrometer testing with side to side difference and Lachman test were used to assess postoperative anterior knee laxity.
Pivot shift tests were also used for rotational knee laxity. Data from roentgenograms reflected the correlation with clinical testing.
Mean value of the side to side difference was 1.3mm. In pivot shift test, the average lateral angle of the reconstructed ligament of negative group was 73.2o , while positive group was 77.2 o , it was statistically significant. The average lateral angel and A-P angle of the reconstructed ligament with inside out technique group was larger than those of outside in technique group.
Recent recommendations placing the tibial tunnel more posterior results in a lower incidence of graft impingement, but we found a relationship between the angle of the reconstructed ligament and rotational stability of the knee.
Anterior-posterior stability can be obtained by achieving posterior placement of the reconstructed ligament. More vertical graft angle caused by posterior placement of tibial tunnel should affect rotational stability. Inside out as the way of fixation technique for the femoral tunnel showed a tendency of more vertical graft angle.
The purpose of this study is to clarify optimal timing of anterior cruciate ligament (ACL) reconstruction from the point of view of meniscus injury.
One hundred thirty-five ACL injuries (under 40 years of age) were analyzed in this study. All knees had undergone primary reconstruction without other ligament injury, and follow-up arthroscopy. ACL reconstruction was performed by the semitendinosus and gracilis method. The rehabilitation protocol was based on that of Shelbourne. Cases were divided into 4 groups by the period from injury to reconstruction. Nineteen knees were of the acute phase, which is within 1 month from the injury to reconstruction. Thirty-one knees were of the subacute phase, which is from 1 month over to reconstruction. Thirty-one knees were of the subacute phase, which is from 1 month over to 3 months from the injury to reconstruction. Forty knees were of the subchronic phase, which is from 3 months over to 1 year from the injury to reconstruction. Forty-five knees were of the chronic phase, which is over 1 year from the injury to reconstruction. We compared arthroscopic findings as well as clinical follow-up results of each phase.
The rate of lateral meniscus injury were 84% in the acute phase, 39% in the subacute phase, 58% in the subchronic phase, and 51% in the chronic phase. The rates of medial meniscus injury were 32% in the acute phase, 29% in the subacute phase, 53% in the sub-chronic phase, and 60% in the chronic phase. Horizontal tear and degenerative tear of the lateral meniscus were increased with time. Osteoarthritic change at follow-up arthroscopy was observed 3 knees in the acute phase, 4 knees In the subacute phase, 8 knees In the subchronic phase, and 13 knees in the chronic phase. There was no difference between clinical results of our ACL reconstruction in the acute phase and chronic phase.
ACL reconstruction in the acute phase was the effective method for preventing secondary osteoarthritis after medial meniscus injury.
Clinical investigations and tests need to be validated by studying their inter-observer and intra-observer errors, but there has been no documentation of such verification in diagnostic knee arthroscopy. We performed a prospective study to find out to what extent the findings in knee arthroscopy differ between two different surgeons.
Two senior specialist registrars (M.S. and A.J.) who took part in this study worked with the senior author (ACW) for a period of eight and seven months respectively. A total of 78 knee arthroscopies admitted from routine waiting list were studied. The specialist registrar first performed arthroscopy when the supervising consultant stayed away from the operating room. His findings were recorded on a proforma by an independent third person before the consultant returned to the operating room and repeated the EUA and arthroscopy without prior knowledge of the trainee findings. Findings from the consultant arthroscopy were then recorded separately on the same proforma.
The following findings were recorded:
Examination under anaesthesia Meniscal pathology ACL pathology Articular surface pathology (more than 1 Outer-bridge grade)
The inter-observer variations in diagnostic knee arthroscopy were found to be high. Given the seniority and experience of the two trainee senior registrars involved in the study, and allowing for the Hawthorne effect, the results of the study cast doubt on this procedure being performed un-supervised. It also questions the validity of any therapeutic intervention based on the findings of un-supervised arthroscopies.
The aim of this longitudinal study is to compare the clinical outcomes of endoscopic ACL reconstruction with either a 4-strand HT or PT autograft over a 5-year period.
90 patients with isolated ACL rupture received PT autograft and 90 received HT autograft were studied annually for 5 years. Assessment included the IKDC Knee Ligament Evaluation, KT1000, Lysholm Knee Score, thigh atrophy, kneeling pain, hamstring pain and radiographs.
The median Lysholm Knee Score was 96 for the PT group and 95 for the HT group. No significant difference was found for subjective knee function, overall IKDC assessment, Xray findings, manual ligament KT1000 instrumented testing, graft rupture or contralateral ACL rupture. There was an increasing incidence of fixed flex-ion deformity seen in the PT group. There was no difference in the requirement for subsequent surgery. The incidence of kneeling pain at 5 years was significantly higher in the PT group.
Endoscopic reconstruction of the ACL utilizing either autograft can restore knee stability and is menisco protective despite a high level of sporting activity. We did find a worrying trend towards an increasing incidence of fixed flexion deformity with time in the patellar tendon group. Kneeling pain also remains a persistent problem in this subgroup.
This study set out to determine the incidence of avulsion of the posterior horn of the lateral meniscus in isolated Anterior cruciate ligament injuries.
Anterior cruciate injuries are often associated with meniscal injuries and a number of different patterns of injuries are described. Although avulsion of the posterior horn of the lateral meniscus has been reported in combined ACL/MCL injuries this has not been reported in isolated ACL injuries. We examined 25 consecutive patients who had ACL ruptures and recorded the presence or absence of an avulsed posterior horn of the lateral meniscus. The mechanism of injury was also recorded. We found 6 patients (24%) with avulsion of the posterior horn of the lateral meniscus from its tibial attachment. All these patients had an external rotation injury rather than a valgus type injury.
Avulsion of the posterior horn of the lateral meniscus is a relatively common finding in ACL injury. If this injury occurs the normal load sharing function of the meniscus may not be present and this may be part of the explanation for the development of degenerative change in the ACL injured knee.
The purpose of this study was to establish the return of function to an unstable knee following stabilization of the anterior deficient cruciate ligament.
15 consecutive cases of chronic anterior cruciate ligament rupture with instability were studied prior to stabilization by patellar bone-tendon-bone autograph, and again at three months post-operation and at one year post stabilization. There were two women and thirteen men in this study. All operations were performed by one of the authors (John Fleetcroft).
Peak torque, total work and average power were studied at 90°/sec and 120°/sec.
Three patients had unusually low contralateral flexor power at 120°/sec pre-operatively, these measurements were excluded from the 120°/sec results.
Our findings show an initial decrease of strength three months postoperatively; on the extensors more than on the flexors.The flexors recovered faster than the extensors.
Extensor function showed a deficit of 13% at both speeds pre-operatively. Three months following surgery this has increased to an average of 33.7% at 90°/sec and 22.8% at 120°/sec. At one year the deficit had decreased dramatically to 2.2% at 90°/sec and 0.14% at 120°/sec.
Flexor function at 90°/sec showed a deficit of 6.4% pre-operatively, 15% at three months and 1.7% at one year. At 120°/sec, pre-operative flexor deficit was 3.1%, +0.16% at three months and +4.4% at one year.
These tests demonstrate the return of function to unstable cruciate deficient knees, an important observation for those wishing to return to sport.
Defects of the anterior cruciate ligament have been treated surgically with intra- and extra-articular procedures since several decades, either as direct repair or using autografts of the hamstring or patella tendon in open or arthroscopic operations. On the other hand there are studies about successful results of conservative treatment available, too.
Casteleyn et al (1) reported about the follow up of at least five years (mean 8.5 years) of 109 patients which excluded professional and high level athletes. The evaluation of their symptoms with an IKDC score showed 23% in grade A and 50% in grade B out of four possible grades with an incidence of 5.4% secondary ACL surgery.
In an editorial article about anterior cruciate ligament reconstruction Dandy et al (2) reviewed the results of several studies about intra- and extra-articular procedures, which examined pivot-shift and restriction of activity.
Johnson et al (3) found in 87 patients with bone-patellar tendon-bone reconstruction and a mean follow up of 7.9 years 26% positive pivot shift and 25% of the patients had unrestricted activity. Sandberg et al (4) reviewed a similar group of 89 patients after seven years with 11% positive pivot-shift and 24% unrestricted activity.
In comparison to these results extra-articular procedures show a higher incidence of pivot-shift and lower levels of unrestricted activity; Odensten et al (5) report 59% clinical instability four years after Ellison procedure and 39% positive pivot-shift with only 44% unrestricted sport activity at six years after MacIntosh operation.
Over the last years extra-articular procedures were abandoned in favor for intra-articular operations.
Today bone-patellar tendon-bone grafts are widely used for these repairs.
Clancy et al (6) and Butler et al (7) have shown in animal studies a decrease of strength and mechanical properties postoperatively during an initial period of revascularisation and remodelling.
Grontvedt et al (8) look at these properties in their study about the effects of the use of a ligament augmentation device by isokinetic testing on a Biodex™ system. They measured peak torque and total work and found a deficit in the quadriceps strength in comparison to the uninjured knee of 25% at six months, 15% at one year and 10% at two years. The hamstrings improved to equal levels already after six months.
The aim of our study was to assess the mechanical properties torque, total work and average power of the hamstrings and quadriceps in order to evaluate the progress of the patients postoperatively including the above mentioned initial decrease in strength. The testing was performed with a Cybex™ machine preoperatively as well as three and twelve months postoperatively.
We tested patients who had a bone-tendon-bone anterior cruciate ligament reconstruction performed between March 1998 and January 1999. It was only a limited time window available for this study and therefore we could conduct the tests only on 15 consecutive patients. We tested two women and 13 men. Their mean age was 38.4 years (21 to 50). Injuries of the anterior cruciate ligament were confirmed by both clinical and arthroscopic examination. Indications were clinical instability, pain and / or swelling during sport or other physical activity and / or other relevant history (knee gives way). All the operations were arthroscopic assisted procedures. They were performed by only one surgeon (J P Fleetcroft). The graft was obtained from the middle third of the patellar tendon and fixed with Acufex™ interference screws.
The isokinetic tests were performed preoperatively, then three months postoperatively and one year postoperatively. The following parameter were obtained for both flexors and extensors at two speeds (90°/sec and 120°/sec): peak torque, total work and average power. At the preoperative test both injured and contralateral knees were tested, at three months and one year only the involved knee. The figures of the uninvolved knee were used as references to calculate mean deficit / progress percentages for the operated side during the course of the study.
Three patients (number 2, 6 and 14) showed at the preoperative measurements unusually low strength at the 120°/sec tests of the flexors of their uninjured knees. The figures of the uninjured knees had to be used as references in the evaluation of progress / deficits of the injured and operated knees. Therefore all calculated results of those three patients became unrealistically high and did not represent true values. As the mechanical properties of the uninjured knees were otherwise of no interest for this study we decided to exclude these patients from the 120°/sec flexor tests.
Preoperatively the extensors showed a deficit of strength (average of peak torque, total work and average power) at both speeds of 13%. This deficit worsened at three months to 33.7% at 90°/sec and 22.8% at 120°/sec. After one year strength had improved nearly to the preoperative level with a deficit of 2.2% at 90°/sec and 0.14% at 120°/sec.
Flexors: The flexors showed smaller deficits than the extensors. Preoperative figures show deficits of 6.4% at 90°/sec and 3.1% at 120°/sec. At three months the deficit at 90°/sec worsened to 15% but at 120°/sec it improved to the level of the unoperated leg (+0.16%). After one year the strength was at both speeds better than at the unoperated leg (+1.7% at 90°/sec and +4.4% at 120°/sec). The detailed deficit / progress figures for all the measured properties of our study are shown in the tables below.
Table 1 Mean deficit / progress [%]; PT = peak torque, TW = total work, Pow = average power
Table 2 Deficit / progress [%] of strength (average of peak torque, total work, average power)
The strength deficits which resulted from the anterior cruciate ligament defect improved significantly. In both muscle groups and at both test speeds the average strength of the operated knee was after 12 months at about the same level as the uninjured leg. As the flexors are to a lesser extent effected by the operation than the extensors they recovered faster; similar to the findings of Grontvedt et al (8).
The flexors showed at both speeds slightly better results than the uninvolved knee and only the extensors had still a small deficit of 0.147% (120°/sec) and 2.21% (90°/sec) in comparison to the uninjured knee after 12 months.
Further could be shown that apart from flexors at 120°/sec an initial decrease in strength occurred at the three months measurements (as also reported in [6] and [7]).
Grontvedt et al ( 8) still report about 25% weakness of the extensors after six months. In our study already at three months all groups apart from the extensors at 90°/sec (−33.7%) have results better than this (−22.8%, −15.04%, +0.17%). Grontvedt’s study shows 15% deficit after one year and 10% after two years. In comparison to this we could demonstrate nearly normal results (−2.2%, −0.14%, +1.7%, +4.4%) after 12 months. As the test speed influences the results especially during the initial period of decreased strength and Grontvedts study tested at 60 and 240°/sec this might be one reason for the different results.
The overall figures for the patients’ progress are satisfactory. They demonstrate the return of function to an initially unstable cruciate deficient knee.
We would suggest further research into the details of the initial weakness during the first postoperative months as this might have implications for physiotherapy and rehabilitation as well as surgical technique and devices.
Tunnel placement in Anterior Cruciate Ligament (ACL) reconstruction is the single most important variable that a surgeon can control in order to achieve a successful outcome. The femoral tunnel is more critical than the tibial.
Audit tunnel positions after ACL reconstruction in a regional centre.We studied 114 patients undergoing primary isolated ACL reconstruction within a 12-month period. Case notes and radiographs were reviewed retrospectively. Tunnel position was assessed on lateral and AP radiographs of the knee. A review of literature established optimal tunnel position. Measurements of tunnel position were made according to the methods described by Jonsson.
16 surgeons (8 consultants and 8 registrars) performed 57 arthroscopic and 57 open reconstructions, using 24 hamstring and 90 bone-tendon-bone autografts. Femoral tunnel drilling was through the medial arthroscopic portal (24) or the tibial tunnel (90). 85 sets of radiographs were available for review (21 not performed post-operatively, 8 not found)
In the sagittal plane, the femoral tunnel insertion should be within the posterior third along an extended Blumensaat’s line and the tibial tunnel between 41 and 49% along the tibial joint line from anterior to posterior. In the coronal plane, the tibial tunnel should exit between 41% and 49% along the tibial joint line, from medially. Our results showed that 65% of femoral tunnels were outside this position, 23% of the tibial tunnels out in the sagittal plane and 55% out coronally. Of those drilled through the medial portal, only 5% of the femoral tunnels were outside our recommended position.
Clinical Governance demands that guidelines for best practice are established and that audit ensures these standards are met. Anatomical studies give useful data in determining acceptable standards, as demonstrated in our audit. To enable this it is imperative that post-operative radiographic assessment is performed routinely.
Ultra high molecular weight polyethylene (UHMWPE) was introduced into clinical practice by Charnley in November 1962 and has remained the standard material for the hip and other total joint arthroplasties.
Wear of the UHMWPE cup, although studied from the beginning, did not appear to be a clinical problem although Charnley suspected that this would be so in the long term.
A review of the outcome of the Charnley low-friction arthroplasty in patients under the age of 40 years at the time of the operation has shown that the incidence of cup migration was exponentially related to the depth of cup penetration. A prospective study using 22.225 mm alumina ceramic (Al 20 3 ) head articulating with cross linked polyethylene was set up with the initial penetration of 0.2 – 0.4 mm in about 2.5 years with no further penetration. The clinical results mirrored closely the experimental results obtained with the identical set of materials and design. The clinical results have now reached 14 year follow-up and the initial total penetration of 0.2 – 0.4mm has remained unchanged.
Review of long term results of the Charnley LFA has shown a mean penetration rate of 0.1 mm/year (0.02 – 0.6). With a mean penetration rate of 0.1 mm/year, the revision rate for cup wear and loosening in patients under the age of 50 at the time of the LFA, and with a follow-up to 32 years, is in the region of 10%. If the penetration rate remained at 0.02 mm/year or less then no cups have been revised for aseptic loosening. Ceramic / UHMWPE articulation is the next stage of evolution of the Charnley LFA. A prospective study using zirconia 22.225 mm head is approaching 7 year follow-up in over 1000 cases.
We retrospectively analysed three hundred and one infected total hip replacements. Infection was defined on the basis of the surgeons clinical impression. This included a thorough history and physical examination, laboratory and radiographic evaluation. Peri operative findings were also taken into consideration.
Despite the overt appearances of sepsis fifty seven of these three hundred and one cases demonstrated no bacterial growth. These were excluded from the microbiological analysis.
The remaining two hundred and forty four cases oven bacteriological evidence of deep infection. Thirty seven cases grew two different organisms both of which were felt to be clinically significant. The remainder grew a single organism. Hence a total two hundred and eighty one bacteriological isolates were grown.
Coagulase negative staphylococcus accounted for 54.8%, staphylococcus aureus 13.5%, streptococci 8.9%, Escherichia coli 6.1% and diptheroids 2.5%.These organisms were plated out in a standard fashion against a variety of antimicrobial agents.
We analysed ten antibiotics and their sensitivity profiles against the spectrum of organisms demonstrated by this series.
Best antimicrobial coverage by a single antibiotic was afforded by fucidic acid (85.3%) and erythromycin (79.6%). Gentamicin was found to be sensitive to only 76.1% of the bacteria present at the time of revision for deep infection.
Combining gentamicin with other antibiotics improved the theoretical coverage. A combination of gentamicin and fucidic acid demonstrated a 97.5% coverage. Gentamicin with erythromycin gave 95.2%.
When treating the infected arthroplasty it may be beneficial to add extra antibiotics to bone cement. This may either be to the cement spacer in a two stage revision or to the definitive cement in a single stage revision. We would suggest that fucidic acid or erythromycin would be good candidates for this. These candidates should also be considered when designing the next generation of combination antibiotic acrylic bone cements.
Periprosthetic osteolysis has attracted attention as a cause of loosening after arthroplasty. The aim of the present study was to examine inflammatory cell localization and the occurrence of apoptosis in granulation tissue from patients who required revision arthroplasty due to loosening caused by osteolysis.
7 patients were studied comprising 3 patients who underwent FHR and 4 patients who underwent THR. Their mean age at the time of surgery was 63.6 years. The mean period from their previous operation to revision was 8.8 years.
Granulation tissue was collected from around the loosened implant fixed in 4% paraformaldehyde and embedded in paraffin. Sections were cut and were first stained with hematoxylin and eosin. Next, immunohistochemical studies were performed using the avidin-biotin complex method. CD45 was used as the primary antibody to detect T cells, and CD68 was used to detect macrophage-like cells. The activity of the macrophage-like cells was assessed with anti-I-NOS and anti-MMP-9.
Apoptosis was investigated using anti-single-stranded DNA (ssDNA). Using another granulation tissue was stored at −80%C, DNA was extracted, and the presence of DNA fragmentation was detected by agarose gel electrophoresis.
Vascularization and infiltration by a large number of inflammatory cells were seen along with large multinucleated osteoclas-like cells. Immunohistochemical studies revealed CD45-positive cells primarily around the blood vessels. The CD68-positive cells were mainly multinucleated cells. The multinucleated cells were i-NOS-positive in 4 patients, and were MMP-9-positive in 5 patients.
The nuclei of many of the multinucleated cells were positive for ssDNA. Agarose gel electrophoresis of DNA showed a marked ladder pattern at the 170 base pair region. This finding indicated DNA fragmentation or apoptosis.
Apoptotic cells were seen in granulation tissue harvested from around loosened implants suggesting that apoptosis may play a role in the pathophysiology of osteolysis.
Our purpose was to evaluate the incidence of anterior knee pain after ACL reconstruction and the associated affecting factors.
The study assessed 50 ACL reconstructed knees: 29 males and 21 females. The age at surgery was from 14 to 39 years old, with 23.7 years old on the average. The ACL injury was unilateral in all cases, and the normal side was defined as the control. We treated chronic ACL-deficient knees by reconstruction of the ligament through a limited arthrotomy using one-third of the patellar tendon (BTB) with the Kennedy LAD as a graft. Anterior knee pain was classified into 4 group: absent, trace-mild, moderate, and severe. We evaluated the height of the patella, knee extension strength, anterior laxity, leg rotation, Lysholm score, and loss of extension. Anterior laxity and leg rotation were measured by a three-dimensional analyzer.
Ten of the fifty knees (20%) had anterior knee pain. Knee extension strength (reconstructed side/control side) was 71.1% in the cases with anterior knee pain and 84.2% in the cases without anterior knee pain. A significant difference was found between these values. Regarding leg rotation, 4 knees showed normal leg rotation (physiological screw home movement) in the cases with anterior knee pain, compared to 31 knees in the cases without anterior knee pain. There was a significant difference in the incidence of anterior knee pain between the cases with normal leg rotation and the cases without. Other factors failed to show any significant correlation. In this study, knee extension strength and leg rotation had a correlation with anterior knee pain.
This is a retrospective assessment of the performance of a consecutive series of the titanium uncemented Gemini femoral component. The Gemini uncemented stem (De Puy) is a modular titanium femoral stem with a cobalt chrome head. It has proximal porous coating allowing stable fixation by bony in-growth and a smooth distal stem allowing mechanical fixation.
Using a direct lateral approach, 152 consecutive patients underwent a total hip replacement using the Gemini uncemented femoral component and an unce-mented cup. Patients were regularly assessed clinically (Harris hip score) and radiologically (Engh’s criteria for fixation of the prosthesis). Kaplan Meier survivorship analysis was used to assess survival.
16 patients were lost to follow-up and 30 were dead with the THR in situ, leaving 106 hips for final analysis, at a mean follow-up of 106 months. The mean age of the group was 60 years (range 25–83) and OA was the commonest diagnosis. The mean Harris hip score improved from 34 to 92(range 83–100). 7 stems have been revised, four of which for aseptic loosening and a further two are radiologically loose. Mean time to revision was 41 months (range 14–76). By Engh’s criteria, 90% of the hips had stable bony fixation; only 4% of the patients complained of thigh pain at final follow-up. Kaplan Meier survivorship analysis with aseptic loosening as endpoint indicated a survival of 93% at 8 years.
A mid-term result with the Gemini uncemented stems at a mean follow-up of approximately 9 years was excellent. This is in sharp contrast to the cemented stem of similar design, even though the uncemented version was used in younger and more active group of patients. Titanium alloy is biocompatible allowing for excellent bony in growth, making it an ideal alloy in the manufacture of uncemented stems. Having a modulus of elasticity close to that of bone explains the low incidence of thigh pain.
The aim of this study was to review the results of the R. Mathys Isoelastic total hip replacement as for five years in this institution.
For the purposes of this study the patients were invited by letter to attend a review clinic. An examination of the hip was made and hip scores calculated. An up to date radiograph was performed and radiolucent lines assessed in comparison to the initial postoperative radiograph.
78 hips in 64 patients were identified from the records. 5 patients had died before review and 18 hips had been revised. Of the patients who died, none had died in the immediate postoperative period and all the deaths were of unrelated causes.
The revised hips were revised for aseptic loosening in 17 cases and infection in one. The mean time to revision was 53 months. All the loosening was femoral.
In the reviewed patients the mean length of follow up was 101 months.
The mean Harris score was 80.3. The mean Merle d’Aubigne score was 13.6. Significant lucent lines were noted in 2 acetabular components and 22 of 43 femoral components.
Life tables were constructed with both best and worst case scenarios. The end point for failure was taken as revision or the date revision was planned. A further set of life tables were constructed adding radiological signs of failure to the criteria.
Survivorship was, at best, 53% at ten years. If radiological failure is taken into account and lost to follow-up patients are counted as failures, “the worst case scenario”, the rate falls to 18% at ten years. A second important finding was that a large number of the patients were subjectively happy with their hip and had been discharged from clinical follow-up in spite of deteriorating radiographs
We feel that this is a poor implant, which needs ongoing clinical and radiological review, and cannot recommend its further use.
This study constitutes the minimum 5-year follow-up (mean 8.8 years; range 5 – 11.5 years) of a consecutive series of 40 proximal femoral allografts performed for failed total hip arthroplasties using the same technique. Nine of these cases had been two stage reconstructions for the management of infected total hip replacements with bone loss. In all these cases the stem was cemented into both the allograft and the host femur. The host bone was resected in 37 cases, and the greater trochanter reattached with a cable grip in 33 cases and with wire and mesh in 3 cases.
The patients were reviewed by an independent observer. There were 4 early revisions (10%): one for infection, one for non-union of the allograft host junction, and two following revision of a failed acetabular reconstruction. Three further acetabular revisions have since also been performed. Junctional nonunion was seen in 3 cases (8%), two of which were managed successfully with bone grafting and bone grafting and plating respectively. Instability was observed in 6 cases (15%). Trochanteric non-union was seen in 17 cases (42.5%) and trochanteric escape in 10 of these (25%). The mean Harris Hip Score improved from 39 to 79. Severe resorption involving the full thickness of the allograft was seen in 7 cases. This progressed rapidly and silently but has yet to lead to the failure of any of the reconstructions.
Although there was a high early complication rate, the medium term survivorship is excellent, and the clinical outcomes highly satisfactory. The striking observation of severe allograft resorption may be related to a combination of factors. These include the absence of any masking or protective effect that the host bone may have proximally, and surface revascularisation with stress shielding secondary to solid cemented distal fixation. Although continued surveillance is warranted, these results justify the use of structural allografts for selected cases.
This is a retrospective assessment of the performance of the titanium cemented Gemini femoral component. The Gemini stem (DePuy) is a modular titanium femoral stem with a cobalt chrome femoral head. It has a roughened proximal surface finish to enhance cement bonding and a fixed distal centraliser.
205 total hip replacements were performed using a titanium cemented Gemini stem and an uncemented cup. All the operations were performed by a lateral approach using modern cementing technique. Patients were assessed clinically (Harris hip score) and radiologically. Kaplan Meier Survivorship analysis was used to assess survival.
8 patients were lost and 36 patients died with their total hip prosthesis in situ. The average follow-up in the remaining 161 hips was 70 months (range 37–124 months). The average age was 70 years (range 35–91). Osteoarthritis was the commonest diagnosis and majority of the patients was female. Using the Barrack’s criteria for cementing quality, more than 85% of the hips belonged either to grade A or B with an adequate proximal cement mantle. 28 hips have been revised (26 of which for aseptic loosening) and a further ten have been recognized as radiological failures. A small sized stem was used in over 85% of the failures. Mean time to revision was 3.1 years. Survival according to Kaplan-Meier Survivor curves at 6 years was 72%.
There is a high incidence of early failure associated with these cemented titanium stems (28%). The possible mechanism of failure is as follows. The rough surface finish and the flexible titanium alloy are likely to produce large amounts of wear debris and the centraliser which is fixed to the stem probably acts as an area of stress concentration causing accelerated destruction of the distal cement mantle. Based on our experience, the continued use of this cemented stem is no longer justified.
This study was performed in order to review the medium term clinical and radiographic outcome of long stem cemented femoral revisions using second generation cementing technique and identify factors predictive of success or failure.
110 long stem revision hip replacements in 106 patients were performed between 1983–1994. There were 51 males and 55 females of an average age of 69 years with a mean follow up of 6.7 years and a minimum follow-up of five years. Clinical assessment included chart review, and assessment by an independent observer using the Harris Hip Score and the Short Form-36. Radiographic review was performed by two independent observers assessing quality of cementing, loosening, trochanteric union, and heterotopic ossification. The cementing technique was evaluated in both the areas of previous fixation, as well as in the new bone below the tip of the previous stem. We reviewed 93 hips in 90 patients, the remainder having either died or been lost to follow-up. 89% of the patients had improved Harris hip score by more than 20 points. Using the Kaplan-Meier method, fifteen-year survivor-ship was calculated at 92.8%. Three (3.2 %) femoral components were revised, six (6.4%) additional femoral components subsided but were not revised; five of these showed poor cementing technique in the virgin zones beyond the area of the previous stem, and two had cortical perforations. Complications included; 7 (7.5%)dislocations, 6 (6.4%) periprosthetic fractures, 2 (2.2%) infections, and 14 (15%) trochanteric non-unions.
Most reports of femoral revision with cement in revision total hip arthroplasty have shown poor results. However, there are no reports that rely solely on long-stem components. This study shows that long stem cemented femoral revisions have an excellent medium term survivorship, good clinical results and high satisfaction rates. The quality of distal cementing is of great importance, as distal radiolucencies and poor cement technique are predictive of failure.
We report the results of seventy-six Harris Galante Porous Cups (HGP 1) in sixty-three patients treated by Total Hip Arthroplasty (THA) with a diagnosis of avascular necrosis (AVN) of the femur (grade III and IV). The cups were inserted between 1986 and 1994 and followed prospectively. Seventy hips with a follow up of more than five years (mean 7.6 years) were reviewed.
At last review the mean Harris Hip Score was 94 (standard deviation (& dcl001;) .8), preoperatively the mean had been 29 (& dcl001;14.7). Radiographically there was no evidence of acetabular migration. The revision rate of the femoral prosthesis was 8.6%, however only three stems (4.3%) were revised for loosening the rest being revised to allow down sizing of the femoral head. The revision rate for the acetabular prosthesis was 7.1%, (five cups). At the time of revision none of the cups were clinically loose and only required the liner to be changed. The complication rate was low with no deep infections or dislocations and only nine hips, (11.8%) with grade III heterotopic ossification. Survival analysis for both stem and cup at 8 years is 96.3% (confidence interval 91 – 100%), with a worst-case survival of 93.6%, (C.I 87.4 – 99.9%)
Previous studies of patients undergoing cemented THA for the treatment of advanced AVN have reported a high incidence of component loosening. This study shows good medium term results using the Harris Galante Porous cup for acetabular reconstruction with cemented femoral components for the treatment of this difficult problem.
A prospective study of Charnley low friction arthroplasty in patients under the age of 51 at the time of surgery.
1092 patients, 668 women and 424 men, mean age 41 years (12–51) at the time of surgery had 1434 Charnley low-friction arthroplasties carried out between November 1962 and December 1990. At mean follow-up 14.2 years (1 – 32), 742 patients (973 hips) are still attending and patients’ satisfaction with the outcome is 96.2%. Survivorship was 95.24% at 10 years and 58.67% at 27 years.
Patients who had had previous hip surgery had revision rate 24.8% compared with 14.1%. Patients with rheumatoid arthritis had fewer revisions than those with developmental hip dysplasia or primary osteoarthritis. Large 43 mm diameter cup gave lower revisions for aseptic cup loosening as compared with 40mm cup. Presence and preservation of subchondral plate, rim support compared to medialization of the cup, use of acetabular cement pressurizer and the reduced diameter neck (10mm) all made a contribution to reducing the incidence of revisions for aseptic cup loosening. Closing the medullary canal with bone block reduced the incidence of aseptic stem loosening. Use of the brace reamers did not affect the outcome and there appears to have been no advantage with the flanged stem.
The long-term problem was the increasing incidence of revisions for aseptic cup loosening. This was exponentially related to the depth of cup penetration by the head of the femoral component.
The long term clinical results of the Charnley LFA remain excellent even in young patients. Rim support of the cup, preservation of the subchondral bone of the acetabulum, cup flange and pressurising of the acetabular cement all make a significant contribution. Distal closure of the medullary canal and central position of the stem are of benefit, but reaming the medullary canal to cortex must be avoided. The long-term problem has been highlighted again as: wear and cup loosening.
We investigate the hypothesis that normal spinal shape is genetically determined raising the possibility that individuals with scoliosis may inherit an ‘at risk’ spinal shape leading to the clustering of scoliosis within families.
A large scale study of spinal topography (Quantec system) in straight-backed sibling pairs of schoolchildren was undertaken. All children had no family or past history of spinal pathology and passed a modified Adams forward bend test. 223 sibling pairs were scanned including 28 heterozygote and 11 homozygote pairs. Control groups were constructed by breaking the sibling pair and replacing the removed sibling with an age, sex matched, unrelated counterpart. A sagittal spine line was extracted and analysed using principal component analysis to produce four scores accounting for 97.5% of the cumulative variation in shape. The scores were analysed by intraclass correlation coefficients (ICC).
The results for the second score were:-
All sibling groups showed greater correlation of sagittal profile for the second principal component than unrelated controls. Significant correlations in shape were seen for both twin groups where no correlation was seen with controls. A significant correlation was observed in same sex pairings. This work suggests that some elements of spinal profile may be familial but also shows correlation with sex. Both of these observations may be important in the aetiology of idiopathic scoliosis.
We assessed the Japanese specific bone age standard with Tanner-Whitehouse 2 (TW2) method for the evaluation of skeletal maturity in adolescent scoliosis.
TW2 bone age was investigated by the left hand-wrist X-rays of 120 girls with adolescent scoliosis. Their chronological age ranged from 10.2 to 19.0 years. Because Risser’s sign is uncertain between Risser IV and V, for comparison of TW2 bone age with Risser’s sign, we classified apophyses that with an apparent narrowing of cartilage and that with a partial fusion as the later of Risser IV. In addition, clinical courses of the skeletal matured cases (adult bones) in 6 months before investigation were reviewed retrospectively. Even or less than 5 degrees change of Cobb’s angle was evaluated as unchanged. Furthermore, bone age distribution of immature cases was also reviewed for comparision of the unchanged group with the progressive group.
None was evaluated as adult bone in the stage from Risser 0 to III. The rate of adult bone which was shown in Risser IV was 43.5%, but 88.9% was in the later of IV. 95.8% of Risser V was already adult bone. Moreover, 93.1% of adult bone was unchanged in their clinical courses. Remaining 4 cases (6.9%) was progressive, but had not progressed in the following 6 months. Bone ages of the progressive immature group distributed in the range from 11.7 to 13.9 years. Those of the unchanged immature group distributed mainly over 13.1 years.
Although it is necessary to follow the immature longitudinally, adult bone appeared almost in the later of Risser IV, and appeared earlier than Risser V. And Cobb’s angle may become unchanged before adult bone. At least adult bone would be an indicator between Risser IV and V.
Side shift exercise was originally described by Mehta. Since 1986, we adopted it for the treatment of idiopathic scoliosis. Outcome of the side shift exercise for the patients with idiopathic scoliosis after skeletal maturity was evaluated retrospectively. Fifty-three patients with idiopathic scoliosis whose curve was greater than 20 degrees by the Cobb’s method were included in the study. All the patients were treated only by the side shift exercise and their treatment was started after skeletal maturity. Skeletal maturity was diagnosed by Risser’s method as either grade IV or grade V. The study comprised five men and forty-eight women. Twenty-six patients had thoracic curve, eight had thoracolumbar curve, and nineteen had double major curve. Patients were instructed to shift their trunk to the concavity of the curve repetitively while they were standing and to maintain the side shift position while they were sitting. In double major curve, larger curve was the subject of the treatment. The average age at the beginning of the treatment was 16.3 years (range, 13 to 27 years), and the average age at final follow-up was 19.8 years (range, 14 to 33 years). The average follow-up period was 3.5 years (range, one to 11 years). The average Cobb angle at the beginning of the treatment was 33.3 degrees (range, 20 to 74 degrees), and the average Cobb angle at final follow-up was 32.2 degrees (range, 10 to 73 degrees). Curves of four patients decreased 10 degrees or more. Most of long term follow-up studies reported that untreated idiopathic scoliosis progressed even after skeletal maturity. Although the follow-up period was much shorter, results of the present study suggested that the side shift exercise was a useful treatment option for the management of idiopathic scoliosis after skeletal maturity.
Ongoing debate exists as to the integrity of the abdominal musculature unit in maintaining spinal support and stability. It is thought that the intra-abdominal pressure generated is important in spine stabilisation. Congenital aplasia of the abdominal musculature, i.e. prune belly syndrome (PBS), might therefore result in loss of spinal function and stability. We discuss the possible role of an intact abdominal musculature mechanism in maintaining spinal saggital balance and its relevance to low back pain with this case illustration of PBS. We also review the literature for the incidence of spinal deformities related to PBS.
We present a unique case of a 33-year-old male with PBS that resulted in loss of spinal saggital balance and development of a thoracic hypokyphotic deformity and thoracolumbar scoliosis. The patient also suffered from mild low back pain. Literature review suggests that secondary scoliosis appears to be the most commonly reported spinal deformity with up to 36% of cases being affected in one study.
Unequal compressive forces on the vertebral end-plates as a result of changes in static rib support, dynamic paraspinal muscle support, and changes in intrathoracic and intra-abdominal pressures may be the proposed mechanisms for the spinal deformities. Compensatory lumbar paraspinal over-activity due to the inability to generate normal intra-abdominal pressures because of a deficient abdominal wall musculature mechanism seems to be the plausible explanation for the thoracic hypokyphotic deformity observed. As a corollary, a failing abdominal wall musculature mechanism has been implicated in the risk for low back pain and its sequelae. Our case implicates that an intact abdominal musculature unit might be important in the maintenance of overall spinal function and stability. Maintaining normal intra-abdominal pressures, and the effects of abdominal exercises on this mechanism, i.e. training specificity, remain an important adjunct to our routine treatment of patients with low back pain.
We perform arthroscopy of the hip in cases like osteoarthritis, aseptic necrosis of the femoral head, rapidly destructive coxarthrosis to exactly locate the site and extent of the lesion of articular cartilage, acetabulare labrum, and synovial membrane. 381 hips in 279 patients were examined by an arthroscopic technique during the last 16 years. Our technique consists of a three directional approach to the hip joint which facilitates a global view of the joint. This three directional anterior, lateral, and antero-lateral approach means the advantage of the swift replacement of the optical instruments and the easy insertion of arthroscopic tools.
Arthroscopic observation is also very useful for academic purposes. Pathological change of cartilage in osteoarthritis of the hip were classified into 4 grades according to the arthroscopic findings. In 113 joints only biopsies for synovial tissue, cartilage or acetabular limbus were performed. Arthroscopic surgical procedures such as joint debridement for osteoarthritis, synovectomy for rheumatoid arthritis, extraction of loose bodies, release of adhesions between the joint capsule and femoral head, and partial resection of the limbus were also carried out in 60 joints with a mean follow-up of 48 months. Average hip score according to Japanese Orthopedic Association achieved in pain point from 6 points to 24 points. With new improved instruments and three-directional technique, hip arthroscopy is rather easy to perform and less traumatic to the patient therefore we believe that it is suitable procedure for the relief from the coxalgia caused by osteoarthritis, rheumatoid arthritis, and torn limbus.
Endochondral ossification involves a well ordered sequence of cellular events. Chondrocytes change their morphology and functions and are ultimately removed by the process of apoptosis. A variety of apoptotic-related signals have been characterised. These include Fas receptor (FasR)/Fas ligand (FasL), p53 and Bcl family. However, there is little known regarding the activity of these signals in the process of fracture healing. The purpose of this study was to investigate mRNA expression of apoptotic signals using RNase protection assay (RPA) and immunohistochemistry in endochondral bone formation.
BALB/C mice aged 8 to 10 weeks were used for this study. First, a transverse fracture was made in the right tibia. Mice were euthanised at 1, 2 and 3 weeks postfracture. The calluses were harvested and studied for the expression of caspase-8, a key enzyme of apoptosis, and apoptosis inducers: tumour necrosis factor-alpha (TNF-α) and its receptor p55, FasL and Fas receptor (FasR), and TNF-related apoptosis-inducing ligand (TRAIL). Four mice at each timepoint were used for immunostaining of fracture callus. Sections were incubated with primary antibody then labelled by avi-din-biotin complex method. Another four to ten tibiae were used for RPA. Fracture callus were harvested and snap frozen in liquid nitrogen. RNA was isolated by TRI reagent and BCP, and mRNAs expression of apoptotic signals were detected.
At each timepoint, mRNA of caspase-8, TNF-α, p55, FasL,FasR and TRAIL were detected by RPA. Immunostainings clearly showed that those apoptotic-related proteins were expressed by callus chondrocytes. Cartilaginous callus is replaced by woven bone in endochondral ossification. In this process, chondrocytes should be removed by the process of apoptosis in which death factors are elaborated directly in both an autocrine and paracrine manner.
To investigate the underlying mechanism of osteocyte death in osteonecrosis of the femoral head (ONFH).
Although there are a plethora of conditions that predispose to ONFH the underlying mechanism that results in the death of osteocytes is poorly understood. Consequently, treatment for early disease has a variable outcome. Recent investigation has focussed on the role of nitric oxide (NO) in the local control of bone turnover. NO is central to bone cell metabolism and has been implicated in the development of apoptosis.
Bone samples were harvested from the femoral heads of 40 patients undergoing total hip arthroplasty – 20 for advanced ONFH and 20 for osteoarthritis (control group). Immunocytochemical techniques were used to demonstrate evidence of NO synthase (iNOS and eNOS) as a marker of NO production and for evidence of apoptosis.
There was a marked increase in the expression of both eNOS and iNOS in the bone marrow and osteocytes from patients with ONFH secondary to steroids and alcohol with a correspondingly high proportion of apoptotic cells. Very little evidence of either eNOS or iNOS could be demonstrated in the control group and no significant apoptosis could be demonstrated. Samples from patients with ONFH secondary to sickle cell disease likewise had little evidence of apoptosis and a less marked increase iNOS production.
Our findings suggest that sickle cell disease may cause infarction of bone which subsequently leads to osteonecrosis. However, steroids and alcohol, or their metabolites, may have a direct cytotoxic effect upon bone leading to an increased NO production and NO-mediated apoptosis rather than necrosis. Our findings may provide important clues as to the underlying pathway leading osteocyte death. Therapeutic measures aimed at preventing production of toxic levels of NO or by blocking specific pathways in apoptosis may provide effective an treatment during the early stages of ONFH by halting disease progression.
To compare the effectiveness of ALIF, using the Hartshill Horseshoe cage, and Graf ligamentoplasty for stabilisation of comparable severity of degenerative disc disease.
Between 1995 and 1997, 27 patients who had single level ALIF with Hartshill Horseshoe cage [group A], and 28 patients who had single level Graf ligamentoplasty [group B] were assessed by Oswestry disability index, a subjective score, Zung Depression Scale [ZDS], and Modified Somatic Perception Questionnaire [MSPQ]. The two groups were similar in age and sex distribution. The patients were randomized, and procedures were all undertaken primarily for symptoms of back pain, although some patients in each group reported some leg pain. No patients with the ALIF group had any MRI evidence of neurological compromise. Where there was any degeneration at more than 1 level, discography was undertaken (8 patients in each group) confirming an isolated pain source at a single level. The duration of back symptoms and leg symptoms in the two groups was similar. There was some difference in the distribution of the MRI grade of disc degeneration between the 2 groups, but this did not reach statistical significance. Following is the characteristic of the 2 groups:
In this group, Graf ligamentoplasty procedure had a statistically significant better outcome than ALIF with the Hartshill horseshoe cage.
This may be due to the retention of some degree of normal mobility of the affected segments after stabilisation with Graf ligaments. However, at a minimum follow-up of 2 years, these represent only medium term results. There is a potential for a change in the outcome in the long term.
To determine whether systemic nitric oxide production in tourniquet-induced skeletal muscle ischaemia-reper-fusion injury (SMRI) is dependent on release of vascular endothelial growth factor (VEGF), a modulator of nitric oxide cytoprotection in myocardial ischaemia-reperfusion injury.
Mice were randomised (n=10 per group) into: time controls (no tourniquet) and test animals (bilateral hindlimb tourniquet ischaemia). Blood samples were collected in test animals prior to ischaemia and after reper-fusion. In controls, blood samples were collected at the same corresponding time points. Serum VEGF, nitric oxide metabolites (nitrite and nitrate) and the proinflammatory cytokine tumour necrosis factor (TNF)-α (an indicator of systemic inflammation) were determined. At the end of reperfusion, the lungs and muscle (right gastrocnemius) were harvested and tissue injury determined by measuring myeloperoxidase (MPO) activity, a marker of neutrophil infiltration. Data are presented as mean ± SEM and statistical comparison was performed using one-way analysis of variance (ANOVA) with significance attributed to P < 0.05.
In comparison to control animals, muscle (4.9±0.3 versus 4±0.03 units/g of wet tissue; P=0.02) and lung (16.7±1.9 versus 10.4±0.5; P=0.005) MPO activity at the end of repercussion was significantly greater in test animals. The table shows the results with respect to serum cytokine levels and nitricxide metabolites.
These data demonstrate that SMRI results in local and systemic proinflammatory responses. In contrast to myocardial ischaemia-reperfusion injury, nitric oxide production in tourniquet-induced SMRI is VEGF-independent. Alternative mechanisms for nitric oxide production in tourniquet-controlled extremity surgery requires further evaluation.
The most considerable cause of nerve root damage are compression force and stretch force. Many researchers had reported about experimental study of the compression force, but it is difficult to find the report describing the stretch force to the nerve roots. The purpose of this study is to evaluate the physiological reaction of nerve roots of rats nuder stretch force.
The nerve roots were prepared from the cauda equina of 8 Wister rats (weight: 300 – 400g). We investigated the changes in threshold and action potential of the nerve roots under stretch force and compression force.
The threshold of the nerve roots increased and action potential decreased in parallel with stretch force. Also, the threshold and action potential recovered after releasing the stretch force. On the other hand, by compression force, the action potential decreased parallel with compression force, but the threshold did not change with compression force. Ten minutes after releasing compression force, the action potential did not recover as much as before, and the threshold increased rather than control.
The different physiological reactions that occurred between compression force and stretch force are hard to explain by circulation insufficiency, as previously reported (hypoxemia and lack of nutrition). We considered that the etiology of the stretch force might be a change in internal pressure of nerve roots and a structural change in nerve cells.
The physiological reaction of the nerve root under stretch force differed from that under compression force and recovered from the damage after release from stretch force.
Disuse atrophy is the basis for profound physiological changes of the muscles of immobilised limbs. The aim of this study was to use ultrasound to assess the quadriceps musculature and to try and measure atrophy. We monitored the effects of enforced reduction of mobility due to trauma on the intramuscular architecture of the quadriceps using high resolution real-time ultrasonography (HRRTU) in 13 skeletally mature male patients (43.2 years, range 16 to 82 years), with an isolated unilateral diaphyseal fracture of the femur or of the tibia. All patients had undergone interlocked intramedullary nailing (IIN). Using HRRTU, the pennation angles and muscle fibre lengths of vastus lateralis, the cross sectional area (CSA) of the rectus femoris, and the quadriceps muscle layer thickness (MLT) were measured in the injured and the normal contralateral limb. Repeated measurements showed the technique of measurement of the variables used in this study to be highly reproducible. There was a significant difference in the angle of pennation of the vastus lateralis in the nailed (15.4°) and the unnailed limb (21.2°), documenting that muscle atrophy causes a change to muscle architecture that results in a significant decrease in pennation angle (p = 0.0002). The muscle fibre length was significantly different (p=0.002) and there was a significant correlation between pennation angle and muscle fibre length (r=−0.51, p=0.001). There was also a significant difference in the quadriceps MLT (p=0.001) and CSA of the rectus femoris (p=0.0004) implying that the whole of the quadriceps muscle is affected.
We hypothesise that the stiffness of the acetabular component influences the stresses transmitted to bone. Thus stress shielding or stress overload of the underlying host bone may be influenced by the choice of fixation method. In addition, we believe that the so called “brake drum effect” plays a significant role in the development of rim stresses and subsequent failure of fixation.
We have constructed a jig which allows the direct comparison, under controlled conditions, of contact stresses measured behind the acetabular component of polyethylene controls, uncemented metal backe cups and cemented all polyethylene cups, under physiological load. The design of the jig also allows measurement of stresses transmitted to the acetabular rim of the same three prostheses in order to confirm the presence and magnitude of the brake drum effect. The contact stresses are measured by miniature pressure transducers which are inserted through specially drilled holes in the shell of the jig so that the transducer is flush with the prosthesis under test. A total of 6 transducers are arranged in concentric circles radiating away from the prosthetic dome, so that contact stresses may be directly measured in various parts of the acetabular bed under conditions that reproduce as closely as possible the situation in a total hip prosthesis
The results indicate that significantly less stress is transmitted to bone when metal back components are used as compared to cemented components and controls. The data confirms that the brake drum effect occurs in both cemented and uncemented prostheses, leading to at least the absence of compressive forces at the prosthetic rim and in some circumstances tensile forces.
The objective of this study was to compare the wear mode of 100 Mrad PE cups run in a hip simulator to retrieved 100 Mrad PE cups, and to evaluate the efficacy of the PE wear model.
15 In-vitro PE cups: 3 each 0,2.5.50,100 and 150 Mrad (9 channel hip simulator, 6.2 million cycle duration, physiological load profile by Paul, 2000N maximum load at 1Hz using 30% bovine serum). 5 Retrieved PE cups: three SOM cups (Mizuho Medical Instrument Co., COP alloy 28 mm head)-0 Mrad after 8 years of clinical use, two 100 Mrad cups after 15 years of clinical use, two T28 PE 2.5 Mrad cups (Zimmer): 18 years and 13 years of clinical use. The cups were examined using a SEM (Philip XL30 FEG) for wear scar locations and PE wear-topography.
Original machine marks were observed in the weight-bearing areas of the highly cross-linked in-vitro PE. No machine marks were observed for the 0 and 2.5 Mrad in-vitro cups and none were seen in any of the retrieved cups. The formation of more nodules and fibrils in the 0Mrad cups compared to the extensivley cross-linked cups (in-vitro and retrieved) was striking. The frequency of occurrence and length of the fibrils and nodules was dependent on the dose of gamma irradiation. More ripples were formed in the 2.5 Mrad and higher cups compared to the non-irradiated cups (in-vitro and retrieved). The in-vitro cups formed more ripples than the retrieved cups. In general, the SEM features for in-vitro Mrad cups appeared similar to those of the retrieved Mrad cups.
The in-vitro Mrad cups accurately reflected the conditions of the artificial joint in living body. Therefore, comparisons of retrieved PE cups with simulator PE cups appeared to be a very powerful research tool.
(2) SEM observation demonstrated far less wear damage in the extensively cross-linked cups than in the non-extensively cross-linked PE. Thus the extensive cross-linked PE cups appeared to be a significant improvement over conventional PE cups in terms of wear resistance.
Many pathological disease processes are manifested by abnormalities in cellular signalling caused by altered protein expression. Our aims, therefore, were to determine whether ‘’degenerative disc disease’’ results in 1) altered proteome expression and 2) such changes might be used as a marker for the disease process.
Using gel electrophoresis, we analysed the proteome expression of nucleus pulposus (NP) derived from patients with scoliosis (‘normal’) compared to degenerate samples from patients with 1) back pain undergoing spinal fusion (DDD) and 2) sciatica undergoing discectomy (herniated nucleus pulposus or HNP). Normal NP tissue was also obtained from organ donor patients with no previous history of back pain. All samples were investigated in duplicate. Protein concentrations were measured qualitatively by visual analysis in a blinded manner and categorised into high, medium, low or absent. The Kruskal-Wallis analysis of variance was sued to analyse the data. Subsequent proteins of interest were determined on N-terminal protein sequencing.
15 samples each were collected each from scoliosis, DDD, and HNP, but only 4 samples from the organ donor groups. One major protein band difference was observed whose molecular weight was 15 kDa and N-terminal sequence homologous with lysozyme C (lysozyme-C-like-protein - LCLP). DDD and HNP samples exhibited significantly reduced levels of LCLP compared to scoliosis (P< 0.0001). All NP from donor patients exhibited high levels of LCLP, but numbers were too small for statistical analysis. No statistical correlation existed between age and LCLP levels.
The true physiological roles of Lysozyme C remains unclear, but it is a known ubiquitous secretory and hydrolytic protein found in saliva, milk, cerebrospinal fluid and synovial liquid, and thought to function in primary immunity. LCLP loss in degenerate disc tissue might be due to 1) lack of production, 2) increased breakdown through a specific ubiquitin-linked pathway, or 3) polymerisation with tissue-specific amyloid deposition. The inflammatory effects within the NP related to localised LCLP-amyloid deposition offers a plausible hypothesis for patho-physiology of disc degeneration and discogenic pain. Until we determine the true nature and function of LCLP, we are no further in understanding the patho-mechanisms of disc degeneration. Moreover, LCLP loss in the NP of degenerate discs may provide a potential diagnostic marker for degenerative disc disease.
The purpose of this study was to investigate the possible relationship between matrix metalloproteinase-3 (MMP-3) promoter 5A/6A polymorphism and intervertebral disc (IVD) degeneration in the older generation.
One of the important steps in IVD degeneration is disc matrix degradation by matrix degrading enzymes such as MMPs. MMP-3 is one of the potent proteoglycan degrading enzymes and has been suggested to play an important role in IVD degradation. A common 5A/6A polymorphism in the promoter region of the human MMP-3 gene has been identified. This polymorphism was reported to be involved in the regulation of MMP-3 gene expression (the 5A allele has 2-fold higher promoter activity than 6A). We now hypothesize that IVD degeneration is associated with MMP-3 promoter 5A/6A polymorphism.
Forty-nine elderly Japanese volunteers (mean age 74.3 years, range 64–94 years) were studied. Each lumbar disc was graded according to the radiographic classification system of IVD degeneration described by Kellgren and Lawrence. The 5A/6A polymorphism was determined with both single strand conformation polymorphism (SSCP) and polymerase chain reaction with allele-specific primers (AS-PCR).
Two subjects (4%) with 5A5A genotype, 16 (33%) with 5A6A, and 31 (63%) with 6A6A were observed. Genotype was totally independent of age and sex. There was a significantly larger number of IVDs graded 2 and higher in the 5A/5A+5A/6A than in the 6A/6A (p< 0.05). The degenerative scores of lumber discs were also distributed more highly in the 5A/5A+5A/6A than in the 6A/6A (p=0.0029).
Many environmental factors have been reported to accelerate IVD degeneration. Recently, genetic factors have also been highlighted as possible risk factors. The 5A allele of the human MMP-3 promoter is a possible risk factor for acceleration of IVD degeneration in people aged over 64 years old. We conclude that MMP-3 plays a key role in the degeneration of IVD in the older generation.
Ulnar drift is a common deformity in the hands of patients with rheumatoid arthritis. There is little in the literature regarding the value of crossed intrinsic transfer with MCPJ arthroplasty (Hellum 1968, Stothard et al 1991). In addition the significance of recurrent ulnar drift on hand function is unknown. The aim of this study is to assess if the addition of crossed intrinsic transfer to metacarpophalangeal arthroplasty has an effect on the recurrence of ulnar drift and to overall hand function.
This is a retrospective comparative study. 73 hands in patients with rheumatoid arthritis undergoing primary 2nd to 5th metacarpophalangeal joint (MCPJ) replacements were studied. In 28 hands a crossed intrinsic transfer was performed and in 45 hands it was not . A similar splintage and rehabilitation programme was followed in each group. Mean follow up was 50 months.
Ulnar drift and active range range of motion, Sequential Occupational Dexterity Assessment (SODA) functional score, patient satisfaction , grip strength.
The two groups had similar preoperative ulnar drift (crossed intrinsic transfer group mean 27 degrees, comparative group 29 degrees, p=0.44). At follow up the crossed intrinsic transfer group had statistically less ulnar drift (crossed intrinsic transfer group mean 6 degrees, comparative group 14 degrees, p=0.01). There was no difference at follow up in active flexion, extensor lag, SODA score, grip strength and patient satisfaction (both groups had 70% improved function).
Dupuytren’s contracture (DC) is a non-lethal disabling disease, characterised by a progressive fibrosis of the deep palmar fascia, produced by an increased deposition of collagen within the extracellular matrix (ecm). Matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases that degrade ecm proteins. Their activity is regulated by growth factors, cytokines and by specific tissue inhibitors (TIMPs). An imbalance in the normal relationship between expression of MMPs and TIMPs is believed to contribute to the pathogenesis of other fibroproliferative diseases.
We have performed a detailed immunohistochemical analysis of DC tissue which provides the most comprehensive profile to date of the MMP and TIMP expression in DC. Sections were immunostained using antibodies against a panel of MMPs and TIMPs. Normal palmar fascia from patients undergoing carpal tunnel release or from cadaveric hands was used as controls.
There was a marked increase in the expression of MMPs and TIMPs within the different areas of DC tissue compared with controls. Both MMPs and TIMPs were expressed in an angiocentric pattern within areas of hypercellularity (corresponding to the proliferative stages of nodules). In some hypercellular areas expression of TIMP1 and TIMP2 exceeded that for the MMPs. Hypocellular cords, which were predominantly composed of collagen, were weakly immunopositive for MMP-2 and MMP-9, but were immunonegative for TIMPs.
Areas of MMP-1 and MMP-2 expression were more intense in the stroma surrounding nodules, and also within the “invading” DC tissue at the dermo-epidermal junction (DEJ) of the skin. Here expression of MMPs was observed around abnormally high numbers of small blood vessels, beneath the rete ridges of the epidermal layer, and also within foci of inflamation.TIMP1 and TIMP-2 were not expressed within the DEJ. These changes were most marked where clinically there was obvious ‘skin pit’ involvement.
Currently the only treatment for DC is surgical. Alternative non-surgical therapeutic protocols might involve manipulating the fibrotic process pharmacologically, for example by seeking to regulate expression of MMPs and their inhibitors.
Fractures about the radial or ulnar aspects of the base of the proximal phalanx or the metacarpal head represent collateral ligament avulsion injuries. Unlike such injuries in the metacarpophalangeal joint of the thumb these injuries are rare and have received scant attention in the literature.
The results of open reduction and internal fixation, highlighting the surgical approach and technique, of collateral ligament avulsion fractures about the metacar-pophalangeal joints of the fingers are presented.
Over a five year period sixteen patients presented to the hand injury service with the above injury. Thirteen of these fractures occurred at the base of the proximal phalanx. Fourteen were acute injuries and two non-unions. These fractures affected a predominantly young population (average age 24 years) and the majority were sustained during sporting activities. All were treated by ORIF except for one in which the patient declined operative treatment. Metacarpal head fractures are assessed through a standard dorsal approach but as the collateral ligament inserts into the volar - lateral aspect of the proximal phalangeal base access to this fracture is best achieved via a volar approach to the digit. Fractures were stabilized with a single interfragmentary screw.
Surgical fixation gave satisfactory results in fourteen cases. All these patients had a full range of finger movement within 3 weeks. One patient developed symptoms suggestive of RSD. At 3 months review all fractures treated by ORIF had united. The patient who declined surgical treatment developed a symptomatic non-union.
Conservative treatment of these unstable fractures leads to non-union. The surgical anatomy dictates the surgical approach, with fractures at the proximal phalangeal base best accessed via a volar approach. ORIF restores joint surface congruity, establishes union and provides stable fixation to allow early mobilisation and return to normal activities.
Restoration of hand function following division of a flexor tendon remains a significant challenge.
We describe a new method of tendon repair. The first suture is placed in the standard fashion, the second suture is inserted with a round bodied needle to avoid damage to the first repair. This is placed at right angles to the first repair and enters the tendon at the furthest point from the cut tendon end. This suture is then tied with the knot on the surface of the tendon, using 4/0 Ti.cron. The repair is completed with a circumferential continuous epitenon suture, using 6/0 Prolene. This method produces a repair with a four-strand core suture and is referred to throughout this paper as the Evans repair.
Flexor digitorum profundus tendons harvested from pigs were used as the experimental model. They were divided at the mid-point and then repaired using either a ‘modified Kessler’ 4/0 Ethibond core suture, a ‘modified Kessler’ 4/0 Ti.cron core suture or the Evans double core suture. The specimens were then tested to failure on an Instron materials testing machine. This produced a figure for the ultimate tensile strength of each repair.
The average tensile strength for the Ethibond Kessler repair was 33 (range, 27–36) Newtons and that of the Ti.cron Kessler repair was 31 (range 21–43) Newtons. The average tensile strength for the Evans repair was 52 (range 43–60) Newtons, and it is significantly stronger than the two standard Kessler repairs (p< 0.001, Student’s t-test). Even the weakest of the Evans repairs was as strong as the strongest of the standard Kessler repairs.
A randomised controlled trial involving 24 patients ( 32 wrists ), 18 wrists being allocated to the single incision group ( S ) and 14 to the double incision group ( D ), was carried out between 1996 and 1999, after clinical evaluation and complimentary EMG studies. Randomisation was performed by one of the orthopaedic secretaries using an envelope technique on the morning of admission. Mean ages were 49.6 ( 32 to 69 ) and 45.8 ( 30 to 54 ) in the S and D groups respectively. The male to female ratios were 2/12 and 5/7 respectively. The pre- and post-operative mass grip strength was measured by a Jamar dynanometer and assessment of post-operative parameters included pillar pain, scar sensitivity, nerve compression symptoms and return to work.
Pillar pain was significantly less in Group D ( Chi-squared = 8.22; P = 0.004 ).
Return to work was less in Group D ( average = 2.6 weeks ( 1 to 12 weeks )) cf. to Group S ( average = 5.6 weeks ( 2 to 16 weeks ) ). ( Wilcoxon Rank Sum Test P = 0.0004 ). No differences occurred in post-operative clinical symptoms ( P > 0.05 ), scar sensitivity ( Chi-squared = 1.025 ; P = 0.506 ) or mass grip strength ( P= 0.506 ).
The tourniquet time was longer for the double incision technique ( average = 15.3 minutes ( 12 to 18 minutes )) cf. to the single incision technique ( average = 12.2 minutes ( average = 10 to 18 minutes )).
The double incision technique is a safe and easy technique for uncomplicated carpal tunnel syndrome resulting in a significant reduction in pillar pain and a more rapid return to work.
The fingertips are important for not only the function of the hand but also cosmetic reasons. In distal phalanx, arteries especially in zone …Ÿ are less than 0.5 mm in diameter however they can be anastomosed ultramicro-surgically with 11-0 suture.
From 1976 to 1999, I have replanted 463 digits in 337 male and 126 female patients whose ages ranged from 4 months to 80 years, with an average of 32.7 years. There were 312 digits with complete amputation, 151 digits of incomplete amputation, 277 digits with trauma in zone …Ÿ and 186 digits in zone … in which more than six months had passed since the replantation.
The results in zone … amputations was better then in cases of amputations in zone …Ÿ because anastomoses of arteries and viens are more relibale in zone … amputation.
I analyzed the results of zone …Ÿ amputation according to types of injury. The survival rate was 100% in clean-cut amputation, 91.7% in blunt-cut, 66.1% in crush and 67.5% in avulsion. So in cases of crush or avulsion amputation in zone …Ÿ, there is relative indication for replantation.
As for postoperative functional recovery, 95% of the survival fingers are in good daily use, or in some use. Compared with stump plasty, our results of survival fingers are far superior functionally and cosmetically. From a survival rate and functinal point of view, replnatation is definitely indicated in cases of zone …Ÿ amputations by clean-cut or blunt-cut and zone … amputations if technically possible.
The purpose of this study is to introduce our technique of free hand screw insertion for scaphoid fractures and clarify the indications of this procedure.
From 1988 to date, we performed this method in 86 cases (75 males and 11 females). Ages ranged from 11 to 73 years (av.: 29). There were 24 cases of acute stable type, 46 of acute unstable and 16 of delayed fibrous union. Screws used were original Herbert screws in 48, other cannulated type screws in 38.
Using an image intensifier, from a small skin incision over the scaphotrapezium joint, a Kirschner wire is inserted to stabilize the fracture temporarily. The wire is pulled volarward to rotate the scaphoid and a second wire is inserted along the intended line of the screw. With the original Herbert screw, after removing the wire, the screw is inserted free-hand. With the other cannulated screws, the second wire is used as guide pin.
Results of 82 cases with follow-up times over 6 months were reviewed. In one case, bony fusion was achieved but revealed symptomatic malunion. In two cases, bony fusion was not achieved. In one of them, an additional bone graft was performed, and good bony union was achieved. In the remaining 79 cases, good bony fusion and good clinical results were achieved.
The best indication for this method is an acute unstable fracture. For acute stable fractures, we recommend this method for three types of patients: those who cannot accept long term immobilization, those who desire to return to athletic activities as soon as possible, and those who also have another fracture in the forearm. It can also be used in cases of delayed fibrous union when good alignment can be achieved and a bone graft is unnecessary.
The use of musculo-skeletal MRI is increasing at spectacular rate, however there have been few rigorous evaluations of its’ clinical effectiveness. This study was conducted to assess the impact of MRI of the wrist on clinical diagnosis and patient management.
A controlled observational study was performed, in which referring clinicians completed questionnaires on diagnosis and intended management before and after wrist MRI. We analysed 118 consecutive patients referred for MRI of the wrist, to the magnetic resonance imaging units at a regional teaching hospital and a large district general hospital. We assessed: changes in clinicians’ leading and subsidiary diagnoses after MRI; their certainty of these diagnoses; and changes in intended patient management.
Five patients had incorrectly completed requests, ten cancelled their appointments and two could not tolerate the MR examination. Complete follow up data is available for 98/101 patients with correctly completed request forms who were examined. The clinical diagnosis changed in 55 of 98 patients (56%). Diagnostic certainty increased in 23 of the remaining 43 patients (53%). Clinicians reported that MRI had substantially improved their understanding of the patients’ disease in 67/98 (68%) patients. There was a change in management in 46/98 (47%) patients, with a shift away from operative treatment. 28 out of 98 (29%) patients were discharged without further investigation. MRI was similarly effective in a regional teaching centre and a district general hospital.
Magnetic resonance imaging of the wrist influences clinicians’ diagnoses and management plans. These results demonstrate the clinical effectiveness of MRI of the wrist in both a regional teaching centre and a district general hospital.
The U-shaped sacral fracture is a fracture pattern poorly recognized, that is not included in the standard classification of sacral fractures. These fractures are significant as they represent spino-pelvic dissociation, have a high incidence of neurological complications and information regarding modern treatment options is sparse. A number of authors have reported isolated cases or small series of patients with this type of fracture, although none explicitly note the bilateral vertical element that makes them U-shaped and represents spino-pelvic dissociation.
We present four patients with U-shaped sacral fractures. All patients were polytraumatised patients of whom three had jumped from a height in suicide attempts illustrating the high energy required to produce this fracture.
Three patients had ilio-sacral screw fixation, supplemented in one with instrumentation from the lumbar spine to the iliac crest. The other had sacral laminectomy with bony stabilization by instrumentation from the lumbar spine to the iliac crest without ilio-sacral screw fixation.
No complications were encountered as a result of fixation. The fixation devices used essentially represent the local expertise that is available. The ilio-sacral screw technique is minimally invasive and appears to provide satisfactory fixation in our limited experience. However as fracture deformity often involves rotation of the upper sacrum, the use of a single screw may not provide adequate support against the deforming forces or allow reduction of the fracture. Additional ilio-sacral screws will provide some rotational control of the sacral fragment if their safe insertion is possible, if not then the forces should probably be neutralized by an additional device from L5 to the pelvis.
The role of sacral decompression is unclear but may be appropriate in the presence of neurological deficit and a severely compromised sacral canal.
These are complex, rare injuries. We recommend their referral to a specialized pelvis/spinal unit for definitive management.
We review the results of the Gamma nail fixation to elucidate its effectiveness in the treatment of peritro-chanteric and subtrochanteric fractures of the neck of femur.
We report the result of 718 cases of Gamma nail fixation in all such cases presenting at our institution since 1988. 573 cases of peritrochanteric and 145 cases of sub-trochanteric fractures were treated by means of standard and long Gamma nail. Age groups of the patients are from 33 to 99 years. No distal locking screw was used in cases of standard nails. All grades of surgeons were involved. Full weight bearing was allowed on the first post operative day. Cases were followed up for one year.
No intraoperative iatrogenic fracture was encountered. Minimal post operative pain was experienced and mobility was regained early. All fractures healed satisfactorily except the following: 51 cases developed coxa vera deformity; 37 cases of undisplaced fractures of base of greater trochanter were noticed at 6 weeks follow up - all healed spontaneously; 1 case of external rotational deformity occurred in a long nail where no distal locking screw was used. 2 cases of deep infection were treated successfully by removal of nail and antibiotic treatment; 4 cases of fracture at the level of the distal end of the prosthesis, presented at 6 weeks to 2 year period following a subsequent trauma, were treated with exchange of device with long nail. Upward penetration of hip screw 22. No case of metal failure observed.
Gamma nail provides a stable fixation in both simple and complex fractures of proximal femur with a much less invasive tehcnique which allows minimal disturbance of fracture haematoma, less incidence of wound infection and less amount of postoperative pain. Early mobility is regained with immediate and unrestricted weight bearing. Biomechanically also Gamma nail produces a better means of osteosynthesis.
The benefits and risks of early fixation of scaphoid fractures were investigated in 88 patients in the working age group with clear bicortical fractures. Patients were randomised using a random number sheet into 44 who had early internal fixation using a Herbert Screw without a cast and 44 who were treated conservatively in a Colles’ type plaster cast for eight weeks. Patients were reviewed at 2,8,12,26 and 52 weeks with pain severity, tenderness, swelling, wrist movement, grip strength, the Patient Evaluation Measure (PEM) outcome score and x-rays assessed at each visit.
There was no difference between groups for age, sex, nature of injury, dominance, side injured or type of scaphoid fracture. The two groups were similar for pain severity at each of the intervals. Eight of the conservative group and one fracture in the operated group did not unite (p=0.01).
At the 8th and 12th week visits the operated group was better than those treated in a cast for wrist range, grip strength and PEM score (less is better). Thereafter there was no difference between groups.
Patients operated on returned to work at a mean of 6 weeks after their injury compared to 11 weeks for those treated conservatively. There were no serious complications, 6 patients had hypertrophic or itchy scars and one had hypoaesthesia in the palmar cutaneous branch of the median nerve distribution.
Early fixation of scaphoid fractures can be offered as an alternative to cast immobilisation with good early benefits and low risk, however the surgery can be technically difficult.
The aim of the present investigation is to study the status of the blood-nerve barrier in the carpal tunnel syndrome and cubital tunnel syndrome using gadolinium enhanced MRI.
The subjects were 68 patients (92 hands) with idiopathic carpal tunnel syndrome and 21 patients (23 elbows) with cubital tunnel syndrome.
The MRI equipment used was a 0.3-T permanent magnet. Using the SE method, T1-weighted axial images were obtained. Then, we intravenously injected gadolinium for enhanced images. We studied the relationship between nerve enhancement and the symptoms of the patients.
Out of 92 hands with carpal tunnel syndrome, 74 hands (80%) showed enhancement of the median nerve. The patients had 58 hands classified as Grade I (sensory disturbance only) out of which 44 hands (76%) showed nerve enhancement , as did 25 out of 29 hands (86%) classified as Grade II (I + thenar muscle atrophy) and all 5 hands (100%) classified as Grade III (II + disturbance of opposition). Enhancement was more prominent in the patients with thenar muscle atrophy. All 23 elbows with cubital tunnel syndrome revealed enhancement of the ulnar nerve. Two elbows were categorized as grade I (sensory disturbance only), 12 as grade II (I + 1’st inter-osseus muscle atrophy), and 9 as grade III (II + claw finger deformity)
In general, capillaries exist inside the endoneurial spaces of peripheral nerves. Intraneural homeostasis is maintained by the perineurium as a diffusion barrier and by the blood-nerve barrier existing in the endothelium. MRI could demonstrate intraneural enhancement at the site of nerve entrapment where intraneural edema resulted from an increase in the vascular permeability of the endoneurium. We conclude that gadolinium-enhanced MR imaging can detect morphological and functional changes of peripheral nerve in patients with entrapment neuropathy.
Concomitant ipsilateral femoral and tibial fractures result from high velocity injuries and are often associated with other, life threatening, injuries. They are rare injuries in children with few published series, none of which comment on the use of flexible intramedullary nails in the treatment of such injuries.
We present our experience of concomitant ipsilateral femoral and tibial fractures in children and discuss the use of flexible intramedullary nails in their management.
Hospital records and radiographs of 19 such injuries in 18 patients were studied. These cases were divided into three groups based on the method of treatment. Group A: (8 cases) both the femoral and tibial fractures were internally fixed.
Group B: (4 cases) only one out of the two fractures had internal fixation while the other was externally immobilised.
Group C: (7 cases) both femoral and tibial fractures were treated with external immobilisation like external fixators, plaster cast or traction.
Six cases in group A were treated with flexible intra-medullary nailing The mean age was 8.5 years. The average follow up was 3.5 years. All patients were reviewed and assessed clinically following discharge from hospital.
Patients treated with internal fixation of both fractures had a shorter hospital stay and were able to weight bear earlier. Limb length discrepancy was common in conservatively treated patients. Mean limb length discrepancy was 3.8 cm of shortening. A better range of knee movement was observed in patients treated with flexible nail for femoral and tibial fracture. Over all a good result was achieved in 70% of the patients. Using our assessment criteria we found that Group A faired better than the other two groups on all accounts.
Only a few small series of such a rare injury has been mention in the literature. More complications have been reported in children under 10 years of age. In our study we found better results when both tibial and femoral fractures were treated with internal fixation. The out come results in our patients were not related to age.
We found that internal fixation with closed flexible intramedullary nailing of both femoral and tibial fractures was a safe and effective technique and has therefore been recommended.
The purpose of this study is to introduce our treatment by skeletal traction in brace and to report the safety and easiness of this method and low incidence of cubitus varus.
In 1980 we developed a specially designed brace for treating the supracondylar fracture, along with a technique of spontaneous reduction by skeletal traction to develop an easy and safe treatment. The brace is made of plastics and aluminum alloy that are radiolucent. The humeral slide bar with attached axillary pad can be moved up and down to adjust the height of the upper arm for each patient.
From 1980 to 1999 we have treated 190 children with displaced supracondylar fracture of the humerus. Their ages ranged from 2 to 14 years old and average of age was 7 years old. The fractures occurred most frequently between the ages of 5 to 6. More boys than girls were injured and the left elbow were more often than the right. Among 190 cases, severely displaced cases were most common. (64%) and moderate case 20%, mild case 16%. The period of follow up was 6 months to 11 years, mean 4 years.
Placing the arm in the brace with the elbow flexed at right angle, unstable fracture site will be stabilized first. Skeletal traction is performed by a spring through the winged screw. The traction is maintained for three to four weeks. Spontaneous reduction of the displaced fragment can be expected and we emphasize that any manipulative technique is not performed during the treatment at all.
Among 190 patients, cubitus varus occurred in only 3 (1.6%) cases because of technical failure. All patients except one obtained excellent functional results, one had 25 degrees of limitation of the elbow flexion. There were no vascular problems or Volkmann’s contracture and ectopic ossification. The results were satisfactory.
Our treatment utilizing the brace and skeletal traction for supracondylar fracture of the humerus in children is safe and effective in preventing cubitus varus.
Much interest and controversy have arisen regarding treatment and prognosis of unstable pelvic fractures. The choice of treatment should be based to a large extent on the long-term outcome. Residual vertical displacement and sacroiliac joint involvement are often cited as being related to poor outcome. This study attempts to clarify whether residual vertical displacement or location of posterior pelvic ring injury correlate with functional outcomes.
33 patients with unstable pelvic fractures not involving the acetabulum were reviewed with greater than 18 months of follow-up. Iowa pelvic scores and descriptive information about sequelae were administered. Fractures were classified according to Tile as 27 type B, and 6 type C fractures. 9 cases were treated with external fixation and 5 cases were treated open reduction and internal fixation. The amount of residual vertical displacement was measured on plain AP radiographs and graded as 0–4,4–10,10–20, or > 20mm. Location of posterior pelvic ring injury was divided into 3 groups, sacral fractures, sacroiliac fracture dislocations, and transiliac fractures.
Residual vertical displacement correlated with the incidence of LBP to some extent, but the difference was not statistically significant. Location of the posterior pelvic injury correlated with the incidence of neurologic injury and gait disturbance.
There was high incidence of lower extremity fractures associated with the pelvic fractures. The incidence of gait disturbance and Iowa pelvic score were not valid as functional assessment tool.
Residual vertical displacement and location of posterior pelvic injury correlated with the functional outcome to some extent.
A prospective randomised study was undertaken of patients with displaced Colles’ type distal radial fractures. Group 1 underwent bridging external fixation with a Pennig device; group 2 underwent manipulation and plaster immobilisation. All patients were initially treated for 6 weeks and reviewed regularly for 12 months.
At a mean of 7.8 years 86 fractures were available for review (36 treated by fixator and 50 treated in plaster). They were assessed to determine the anatomical and functional outcome of their wrist and also the incidence of post-traumatic degenerative change.
The patients had standard anteroposterior and lateral radiographs taken, to allow standard measurements to be made. The degree of arthritic change was also documented. An independent physiotherapist carried out a functional assessment, consisting of range of movement and grip strength in both wrists.
A Gartland and Werley demerit score was calculated, 94% of patients in each group had an excellent or good outcome. Patient satisfaction was comparable, 94% in the fixator and 92% in the plaster group were entirely satisfied.
Although a significant difference was found in terms of radial shortening between the groups, favouring the fixator group (p< 0.05), shortening of > 2mm did not adversely effect the functional outcome. However bridging external fixation did not improve the dorsal angulation in this study. No other radiological or functional parameter showed a statistical difference between the groups.
One patient in this series developed symptomatic post-traumatic arthritis. Grade 1 radiological signs (Knirk & Jupiter) occurred in 25% of patients but only half of these had sustained intra-articular fractures.
In conclusion: no overall long term benefit has been found to treating Colles’ type distal radial fractures with bridging external fixator as compared to plaster immobilisation.
External fixation of distal radius fractures usually involves the use of a bridging fixator. However, immobilisation of the wrist can be associated with various complications and therefore dynamic external fixators were developed to allow wrist mobilisation with the fixator in place. But dynamic fixators themselves are not without complications and more recently interest has been rekindled in non-bridging external fixators (otherwise called metaphyseal or radial-radial fixators).
Following a pilot study using a non-bridging external fixator (Delta frame) in the treatment of intra-articular distal radius fractures, our aim in this study was to compare the functional and radiological outcome of the Delta frame and a standard wrist-bridging static external fixator in the treatment of such fractures. Sixty patients with intra-articular distal radius fractures were randomly allocated to receive either a static bridging Hoffman external fixator or a non-bridging Delta frame. All patients had the fixator removed at six weeks. Clinical and radiographic assessment was performed regularly up to a maximum of twelve months with the clinical results being expressed in terms of range of movement, pain, grip strength and ability to perform certain activities of daily living. Radiological assessment was performed by an independent radiologist. Mean follow-up was ten months.
The only sustained significant difference in function was a greater range of flexion in the Hoffman group. No significant difference could be detected between the two groups in terms of the radiological outcome. Complications included pin-site infection, paraesthesia, extensor pollicis longus tendon rupture and chronic regional pain syndrome. Three patients underwent further surgery. We did not demonstrate any advantage in the use of a non-bridging fixator in the treatment of intra-articular distal radius fractures.
The use of a forearm cast for paediatric buckle fractures of the distal radius is widespread practice. These fractures do not displace and follow-up in Fracture Clinic is only for cast removal. This may mean missed school for the child, or work for parents.
Modern materials allow a robust lightweight back-slab to be used for protection of these stable, though painful, injuries. Unlike a plaster of Paris backslab, Prelude? (Smith and Nephew) is removed by unwrapping the outer bandage. Parents can do this at home.
We prospectively studied 41 consecutive children aged 12 or less with buckle fractures of the distal radius, presenting to Fracture Clinic. After the diagnosis of isolated buckle fracture was confirmed, a Prelude? cast was applied. Parents were given a full explanation and written instructions, which were also sent to the GP. Telephone follow-up was carried out at 3–4 weeks.
Forty of forty-one parents expressed satisfaction with both the treatment and the instructions. The parents of one patient misunderstood the instructions, re-presented to fracture clinic and were dissatisfied for this reason.
With modern casting materials and adequate instructions at Fracture Clinic, routine follow-up of patients with buckle fractures is unnecessary. Resource savings can be made in this way with no compromise to patient care and increased patient/ parent satisfaction.
Our purpose is to use radiographs to compare callus formation with two types of intramedullary nailing for femoral shaft fractures: reamed interlocking (IL) and Ender nails.
Femoral shaft type A fractures according to AO classification were studied.
From 1991 to 1995, 27 patients with 27 fractures were treated with reamed IL nailing and 79 patients with 81 fractures were treated with Ender nailing. IL group included with an average of 22 (range, 16–28) years, and the Ender group included with an average of 28 (range, 15–72) years.
Patients had been followed for an average of 1.8 (range, 1–2.8) years after surgery. In all cases of IL group, the femoral canal was reamed. For type A3 fractures, an interlocking screw was inserted only at the distal site. For type A1 and A2 fractures, both proximal and distal locking screws were placed. In the Ender nailing cases, 3 to 5 Ender nails were inserted from medial or lateral side of the supracondylar or intertrochanteric regions of the femur as was dictated by the fracture site. All of these fractures were reduced by a closed technique. The measurement of postoperative callus area was calculated from the maximum cross-sectional area on the anteroposterior and lateral radiographs.
Fracture healing was successful in all patients. On the radiograph, the callus for the IL group appeared at a mean of 3.9 weeks after surgery, and at a mean of 2.8 weeks for the Ender group. In the IL and Ender groups, fracture healing was noted at a mean of 3.4 and 2.0 months, respectively. The mean area of callus formation in the IL and Ender nailing was 439.5mm2 and 699.4 mm2, respectively. To compare the two groups by using a Mann-Whitney U test, the significant differences were seen in the callus appearance period (p< 0.05) and in the callus area (p< 0.01).
Dynamization at the fracture site is reported to increase external callus formation.
Our results indicate that the elasticity of the fixation obtained with Ender nailing promotes callus formation.
We developed a new type of bioactive bone cement, CAP (Hydroxyapatite composite resin; composed of 77% w/w hydroxyapatite granules and bisphenol-A glycidyl methacrylate-based resin) for bony defect filling. Elastic modulus of CAP is similar to a cortical bone, while it is injectable before hardening and physiologically bonding with bone in 4 to 8 weeks. We present a new method of treatment for unstable Colles’ fracture with this material in clinical use.
Experimental comminuted Colles’ fracture was produced in three fresh frozen cadavara. Fracture was reduced and fixed percutaneously with K-wires. 4.5mm drill hole was opened on the radial cortex 3cm proximal to the fracture site. Comminuted fragments were pushed-up to the subchondral area with a blunt rod and CAP was injected through the same way. After cement hardening, K-wires were removed. X-ray photos were examined before fracture, after fracture and after reconstruction with CAP, in order to evaluate the shape of the radius. CT was examined to evaluate the placement of CAP.
Radiographic parameters of radii were well recovered after reconstruction with CAP. Over correction of the radial length was observed in one bone but good reduction was generally achieved (Table). This means realignment of the distal radioulnar joint, which results in good outcome clinically. In transverse section of CT, 41 to 69% (average 55%) of subchondral area was filled with CAP. Filling of CAP was better in an osteoporotic bone. These results show the usefulness of this material for treatment of unstable Colles’ fracture especially in osteoporotic patients.
To assess patient/parent satisfaction with treatment of radial Forearm Buckle Fractures without the necessity of fracture clinic visits.
A+E staff were provided with definitions and suitable example X-Rays of radial forearm buckle fractures. The A+E staff were asked to mark the films with a green dot for Radiological review if the patient was included in the study, and these films were seen within 24 hours by a consultant radiologist.
Over a three month period all patients with radial forearm buckle fractures seen in A+E were treated with an Alder Hey splint rather than plaster, they were then given a fracture clinic appointment for three weeks later. At this visit the medical staff completed a proforma with the following information, appropriateness of the diagnosis, side, bone/cortex involved, degree of angulation as well as the mode of injury.
The patients and their parents were asked whether they were happy with the level of support that the splint gave and whether they would have been happy to remove the splint without visiting the fracture clinic.
72 (86.7%) had suffered low energy injuries, 5 (6%) high energy injuries, 5 (6%) did not attend their clinic appointment.
65 of 78 (83%) of parents and 65 of 72 (90%) of patients felt that the level of provided support was adequate (6 patients too young to answer)
58 of 78 (74%) of parents and 53 of 72 (74%) of patients would have been happy to make the decision to remove the splint themselves (6 patients too young to answer)
5 (6%) of the diagnoses were deemed to be inappropriate, of these 2 were picked up in radiology review and sent to clinic and 3 were soft tissue injuries.
We feel that the results show that the majority of patients with radial forearm buckle fractures (appropriate guidelines available to A+E staff) do not need to be seen in the fracture clinic, as long as their X-Rays are reviewed and any inappropriately diagnosed fractures sent to clinic. This has significant implications both for fracture clinic workload and also financially for hospitals.
The main object of acetabular revisions is to restore bone stock and provide adequate support for the cup. Allograft bone has been used to reconstruct the acetabulum with variable results. This study is a prospective assessment of the performance of the uncemented cups with morsellized allograft bone in revision acetabular reconstruction.
A single surgeon using a direct lateral approach performed 98 acetabular revisions. An uncemented hemispherical cup with multiple screw holes and morsellized allograft bones was used in all the reconstructions. Patients were clinically assessed by Harris Hip score. Acetabular defects were classified by AAOS Classification system using standard AP pelvis x-rays. Massin’s criteria was used for assessing cup migration; evidence of screw breakage and acetabular bone incorporation were also looked for.
5 patients died before the 3-year follow-up, leaving 93 hips for final analysis. Mean age at surgery was 66 years (range 24–87). Majority of the acetabular defects belonged to AAOS type III. The mean follow-up was 76. 13 hips have undergone repeat revisions, five of which for aseptic loosening of the cup. Meantime to revision was 42 months.
Reconstruction of the bone-deficient acetabulum in revision arthroplasty of the hip is a difficult problem and no single procedure is universally good. However, the use of allograft bone provides a biological solution by restoring the bone stock. The use of uncemented cups with screws provides the primary stability that is supplemented later by the incorporated allograft bone. The rate of revisions for aseptic loosening of the cup in our series is low at 6% after a mean of 6 years. Even in these cases the repeat revisions were significantly easier due to restored bone stock.
To assess primary and revision knee arthroplasty revision activity in a single English health region, and identify trends and reasons for revision surgery.
Surgeons performing knee arthroplasty surgery in Trent Region (Population 5.13 million: 16 hospitals : 107 Consultant Orthopaedic Surgeons) provide the Trent Arthroplasty Audit Group with patient and operative details by completing a standard proforma. Data capture is optimised by a peripatetic clerk checking theatre and admission records in each hospital
18762 primary knee arthroplasties were performed in Trent Region in the period 1990 – 1999.
949 revision knee arthroplasties were performed between 1992 and 1999.
In the last 10 years the number of TKA’s implanted in patients aged 55 yrs or less increased by 300%, there was a corresponding increase of 380% in patients aged 85 yrs. or over whilst the number of patients who had their knee replaced for rheumatoid arthritis decreased by 59%. 83% of patients are satisfied with their TKA when questioned 1 year post surgery. 52 of the 87 surgeons who perform TKA revision perform less than 1 per year whilst 30% of the revisions are performed by 4 surgeons in this region. The reasons for revision TKA were:
Aseptic loosening
38%
Infection
24%
Implant failure
8%
Instability
7%
Patellofemoral pain
5%
5% of knees revised for infection required further revision surgery for recurrence of the infection.
The Trent Knee Arthroplasty Register has the potential to help us evaluate TKA outcome and set standards in a U.K. settting.
We present the mid term results of 267, 3M Capital hip replacement performed in a single institution from 1991 to 1994. Patients were recalled back to clinic in April 1998 after the reported high failure rate of 3M hips. Fifty- nine hips were excluded from this study for various reasons.
Average follow-up was 68.8 months. Nine (4.2%) have been revised for aseptic loosening at the time of review and further 10(4.8%) of the stems are radiologically loose. There was no statistical significant difference between hips that failed, regarding grade of the operating surgeon, surgical approach: trochanteric osteotomy or Hardinge, or type of prosthesis used: monoblock (stainless steel) or modular (titanium). Acetabular wear rate, width of medial cement mantle or cancellous bone at level of neck at Gruen zone7, or stems with canal fill index less than 50%, 7 cm below the level of the collar also showed no statistical difference. Male patients had higher incidence of loosening (p=0.001) which was statistically significant. Both varus and valgus alignment of the stem had higher failure rate which was significant. We could no find any obvious reason for failure in 10 of the 18 patients. The stem was either in varus or there was an inadequate cement mantle in 8 of the failed hips on the initial postoperative radiograph. A feature of this study was high incidence of endosteolysis and debonding of prosthesis from cement in the failed cases.
The present series showed considerably lower revision and loosening rate of 3M stems compared to the published series, the reason for which is not clear. Only Palacos cement was used in this series, which may partly account for the lower failure rate. Surface finish of the stem leading to debonding of the prosthesis from cement along with different modulus of elasticity probably accounts for the higher rate. Technical failure is partly to blame for the higher failure rate.
To report a 15-year survival analysis of the Oxford Medial Unicompartmental Knee Arthroplasty (Oxford UKA) in an independent series.
We report the results of a series of 420 Oxford UKAs performed between 1983 and 2000. Indications for surgery were primary antero-medial osteoarthritis of the knee with an intact ACL, correctable varus deformity of < 15° and < 15° fixed flexion deformity. The state of the patello-femoral joint was not used as a selection criterion. Patients were contacted by a postal questionnaire or by telephone. The outcome of all 420 knees was established, with none lost to follow-up. Seventy-six knees were in patients who had died and the state of each arthroplasty was determined from hospital and GP records.
Seventeen patients (4%) had required revision. Indications for revision were lateral compartment arthrosis (7), component loosening (4), bearing dislocation (4) and infection (2). There were no failures for polyethylene wear. Cumulative survival at 15 years was 94.3% [95% CI 3.8%]. The worst case scenario was 94.3% as none were lost to follow-up.
The results from an independent series are important, as they avoid bias. The 15-year results of this independent series are better than any other reported series of unicompartmental device at 15 years and as good as the published independent 15 year survival results for total knee arthroplasty. The data illustrates that excellent long-term survival can be achieved with the Oxford UKA, allowing patients to benefit from the advantages that unicompartmental arthroplasty offers. We believe that provided patients are selected appropriately, this device provides the treatment of choice for anteromedial osteoarthritis of the knee.
Cementless fixation for total knee arthroplasty (TKA) has been proposed as an alternative to cemented for several reasons, of which the most important is the possibility of increased survival. The purpose of this study was to compare the ten-year survival of TKA in a unique prospective randomised trial of cemented versus cementless fixation.
A consecutive series of patients was randomised to undergo either cemented or cementless Press-Fit Condylar (PFC®) TKA. There were 219 patients (277 TKA) in the cemented group and 177 (224 TKA) in the cementless group. There were no significant differences in age, gender or diagnosis between the two groups.
A single surgeon (PJG) performed or directly supervised all operations. The prosthesis used in all cases was the posterior-cruciate-retaining PFC® knee replacement system. Independent clinical review was performed at six months, annually until five years, and finally at ten years after surgery. Using revision surgery as the end-point, logrank analysis was used to compare the ten-year survival of the two groups.
The mean interval of follow-up was 6.3 years (range, 2.0–11.7). At the last review, 104 patients (138 TKA) had died, without need for revision. All patients were traced and there was no loss to follow-up. In the cemented group, seven arthroplasties were revised; five for infection and two for exchange of polyethylene inserts. Ten-year survival was 96.5% (95% CI, 90.9–98.7%). In the cementless group, six arthroplasties were revised; three for aseptic loosening, one for infection, one for instability and one resizing for anterior knee pain. The ten-year survival was 96.6% (95% CI, 89.6–98.9%). There was no significant difference in the survival of the two groups.
The long-term survival of cementless PFC® TKA is not significantly different from their cemented counterparts. The use of less expensive cemented implants, therefore, can make a significant impact on health resource planning.
Polyethylene wear can be an important cause of knee replacement failure.
Six TKRs in young, active patients with excellent Oxford Knee Scores and Knee Society Scores, mean 76 months post knee replacement and 5 control patients, 2 weeks post TKR, were selected. Each patient had weight bearing stereo radiographs of at 0, 15, 30, 45 and 60 degrees of flexion while standing in a calibration grid. These x-rays were analysed using our Radio Stereometric Analysis (RSA) system. The three-dimensional shape of the TKR (manufacturer’s computer aided design model) was matched to the TKR silhouette on the calibrated stereo radiographs for each angle of flexion. The relative positions of the femoral and tibial components in space were then determined and the linear and volumetric penetration was calculated using Matlab software.
The accuracy of the system was found to be 0.3mm (CAD model tolerance 0.25mm). The mean linear wear in the control patients was 0.02mm (range −0.19 to +0.23mm). Average linear penetration in the study group was found to be 0.6 mm at 6 years, giving an overall linear wear rate of 0.1mm/year. Average penetration volume at 76 months was 399mm3. The average volumetric wear rate was 63mm3/year.
It is possible to measure volumetric wear in vivo using RSA. Volumetric wear rate was found to be 63mm3 per year. Studies on retrieved normally functioning hip replacements have shown volumetric wear rates of 35mm3 per year. However, clinical outcomes of knee replacements are comparable to those of hip replacements, suggesting that the knee has a more effective mechanism for dealing with polyethylene wear particles.
To document the incidence of intra-articular pathology resulting from delayed Anterior Cruciate Ligament (ACL) reconstruction
A prospective assessment of meniscal and chondral damage found at the time of primary ACL reconstruction, and the relationship of incidence of intra-articular pathology to time since original ACL injury.
We reviewed 1960 patients who had undergone a primary ACL reconstruction. There were 1443 Males and 517 females, with an average age of 28.3 years. The average age at injury was 25.4 years.
1136 patients (58%) had secondary intra-articular pathology, 621 (54.7%) had a medial meniscal tear, 594 (52.4%) had a lateral meniscal tear and 381 (33.5%) had chondral damage. The average time from injury to reconstruction was 2.9 years (34.8 months) Those with secondary intraarticular pathology presented for reconstruction later, average 3.9 years (46.8 months), compared to those without secondary pathology, average 1.5 years (18 months).
The incidence of secondary intra-articular pathology increased with delay between original ACL injury and reconstruction. 41% of those waiting 12 months; 60% of those waiting 3 years; 79% of those waiting 5 years and 88% of those waiting 10 years had secondary intra-articular pathology.
This study confirms the relationship between an unstable ACL deficient knee and the incidence of secondary intra-articular pathology. Furthermore, our study reveals the increasing incidence of meniscal and chondral pathology the greater the delay from injury to ACL reconstruction. To prevent unnecessary secondary intra-articular pathology we recommend ACL reconstruction is performed with minimal delay.
The pathophysiology of discogenic low back pain is poorly understood. The morphological changes occurring in disc degeneration are well documented but unhelpful in determining if a particular degenerate disc will be painful or not.
Herniated intervertebral disc tisssue has been shown to produce a number of pro-inflammatory mediators and cytokines. No similar studies have to date been done utilising disc material from patients with discogenic low back pain.
The aim of this study was to compare levels of production of interleukin-6 (IL-6), interleukin-8 (IL-8) and Prostaglandin E2 (PGE2) in disc tissue from patients undergoing discectomy for sciatica with that from patients undergoing fusion for discogenic low back pain.
Tissue from 50 patients undergoing discectomy for sciatica and 20 patients undergoing fusion for discogenic low back pain was cultured and the medium harvested for subsequent analysis using an enzyme linked immunoabsorbent assay method. Statistical analysis of the results was performed using the Mann-Whitney test.
Disc specimens from both experimental groups produced measurable levels of all three mediators. Mean production of IL-6, IL-8 and PGE2 in the sciatica group was 26.2±75.7, 247±573 and 2255±3974 respectively. Mean production of IL-6, IL-8 and PGE2 in the low back pain group was 92±154, 776±987 and 3221±3350 respectively (data = mean production pg/ml ± 1 standard deviation).
There was a statistically significant difference between the levels of IL-6 and IL-8 production in the sciatica and low back pain groups (p< 0.006 and p< 0.003 respectively).
The high levels of pro-inflammatory mediator production found in disc tissue from patients undergoing fusion for discogenic LBP may indicate that nucleus pulposis pro-inflammatory mediator production is a major factor in the genesis of a painful lumbar disc. This could explain why some degenerate discs cause LBP while other morphologically similar discs do not.
The role of posterior cruciate ligament (PCL) in total knee replacement (TKR) has been a matter of debate for long time and remains controversial. In this study, the effect of posterior cruciate ligament (PCL) sacrifice on the tibiofemoral joint gap was analysed in 30 varus osteoarthritic knees undergoing posterior stabilized total knee replacement. Medial soft tissue was released and bone cut was made without preserving the bone segment of tibial PCL insertion. Then the medial and lateral joint gaps in full extension and 90□& lsaquo; flexion were measured before and after PCL sacrifice using a tensioning device (V-STAT tensor(tm), Zimmer). After PCL sacrifice, the flexion gap significantly increased both in medial and lateral side (4.8 □} 0.4 and 4.5 □} 0.4 mm respectively, mean □} SE) compared to those seen in the extension gap (0.9 □} 0.2 and 0.8 □} 0.2 mm, p < 0.001 ANOVA). There was no significant difference between the changes in the medial and lateral gap (p = 0.493). In conclusion, results of this intraoperative measurement showed that PCL sacrifice leads to a selective increase in the size of flexion gap by an average of 4.7 mm whereas it had little impact on the correction of varus deformity. These findings provided insights as for the role and necessity of PCL sacrifice in the correction of varus and flexion deformity. Because the flexion gap surpassed the unchanged extension gap during PCL sacrifice, PCL release could be used as a surgical technique to balance the gaps without additional bone cut.
The purpose of this paper is to emphasize lateral compartment arthroplasty as efficient method and to discuss postoperative problems by investigating mid-term results (over 5 years)
Two hundred and twenty two consecutive unicompartmental knee arthroplasties (UKA) were performed in our hospital between August 1977 and December 1999. Thirty eight joints of 37 patients underwent lateral UKA. There were 8 male and 29 female patients with an average of 65.1 years old. The following prostheses were used: Marmor in 5 patients, Oxford in 1, PCA in 11, and Omnifit in 21. Out of them, 24 joints had follow up over 5 years after replacement. Three patients died of unrelated illness and 3 were lost to follow up. The remaining 18 joints could be followed from 60 to 189 months (average, 99 months). The knee score of the Hospital for Special Surgery (the HSS knee score) was used for clinical evaluation.
Clinical results by the HSS knee score showed that 2 joints were judged as “good”, 13 as “fair”, and 3 as “poor” before surgery. After surgery 13 joints were improved to “excellent”, 3 to “good”, and 2 to “fair”. The two joints with fair results had revision surgery. In all, 16 joints had satisfactory results. With radiological evaluation, the average preoperative alignment on standing was 14.9o of valgus angulation and corrected to 6.9 o of valgus. Although radiolucent lines under the tibial component were not found, a radiolucent line was observed and extended to loosening in one femoral component. This patient was successfully revised to another type of UKA 3 years after the index surgery. In the medial compartment, we found slight deterioration of osteoarthritic change in 5 joints. Of these, one patient, needed medial UKA.
Lateral UKA is a reliable and successful option compared with other procedures in a patient with low level of physical activity, because the long-term results tend to last and loosening of the tibial components has not been observed as commonly as in medial UKA. However, deterioration of the medial compartment may occur. The alignment after surgery must be in slight valgus for a satisfactory long-term result.
Percutaneous radiofrequency neurotomy of the lumbar medial branch is a widely accepted treatment for pain of the lumber intervertebral joints. However its success rate has varied among authors. One reason for this inconsistency is the lack of method for objective evaluation of whether the nerve has been sufficiently denervated or not. This study has made possible real time and accurate monitoring of whether electrocauterization is properly executed or not.
The subjects were 50 patients with law back pain persisting for 3 months or longer in whom facet block or medial branch block of posterior ramus was only temporarily effective. They ranged in age from 19 to 76 years (mean 54 years) and were followed up for 1 year to 7 years and 1 month (mean 2 years and 9 months). In our percutaneous radiofrequency neurotomy, the target point of denervation is defined as the groove between the mammillary process and accessory process (1) and complex muscle action potentials (CMAPs) of multifidus muscles are used as an index for objective evaluation of the effects of denervation.
Improvements were observed immediately after the treatment in 39 patients (78%). The effects of this treatment, once attained, remained over a long period, and the duration of effects was 18–20 months as estimated by the cumulative success rate calculated using the Kaplan-Meyer method.
Patients must be carefully selected for percutaneous radiofrequency neurotomy to be consistently effective, all the more because the procedure is simple. However, it is a reliable method for denervation of the lumbar medial branch and long-term relief from pain can be expected. This therapy, therefore, is an effective alternative for the treatment of chronic pain due to lumbar intervertebral arthropathy that resists conservative treatments and disturbs daily living.
Back pain may be related to abnormal segmental movement and suggested treatment is segmental fusion. Recent techniques using cages can achieve fusion rates of over 90% but the clinical results are no better. We hypothesise that the cages integrate fully to adjacent vertebrae taking all the load, producing abnormal stress patterns in the vertebrae producing pain.
In this study a simple FE model of a disc and its adjacent vertebral bodies was developed using ANSYS software. The dimensions of the model were based on those of a human lumbar disc. The normal disc was modelled as having nucleus with fluid properties (bulk modulus 1720 MPa). To model the degenerate disc, the material properties of the nucleus were changed to be the same as the annulus (Young’s modulus, E=5 Mpa; Poisson’s ratio, n=0.49). To model fusion of the disc, the nucleus was replaced with a simple representation of a one of three of the commonly used cages. In all the models the material properties of the cancellous bone (E = 100 MPa; n = 0.3) and the cortical bone (E=12000MPa;n=0.3) remained the same. The model was loaded axially with 1.5 kN.
The vertical and horizontal stress patterns around a loaded degenerate disc showed areas of increased loading in the endplate and cancellous bone. The inclusion of cages in the model showed high concentration of tensile and compressive stresses at the point of contact with the cages and in the cancellous bone of the vertebral bodies. The stress pattern showed more similarity to that of degenerate disc, than a normal one.
Fusion cages alter the pattern of stress distribution in the adjacent vertebral bodies from that of the normal disc. The excellent fusion rates of the cages are not mirrored by improvement in clinical results. It supports the concept that abnormal load transfer may be a more significant cause of back pain than abnormal movement.
Surgical repair of rotator cuff tendon is one of the most common orthopaedic procedures performed in the United States. This prospective single-surgeon study reports the long-term results of chronic rotator cuff repair. Vigorous statistical analysis was carried out to detect any association of various outcome parameters with the exact surgical pathology.
105 consecutive shoulders (97 patients) undergoing open repair of chronic (> 3 months) rotator cuff tear between 1975 to 1983 by the senior author were recruited to the study. Pain unresponsive to nonoperative treatment was the indication for surgery. The details of patient’s medical records, radiographic data, and the operative findings were prospectively reviewed. There were 67 males and 30 females with a mean age of 58 years (range, 38 to 75). Follow-up averaged 11 years with no patients lost to follow-up. There were 16 small, 40 medium, 38 large and 11 massive tears.
Surgical repair relieved pain in 92% of patients (p<
0.0001). There was also a significant improvement in range of motion (p<
0.0001) and strength of abduction and external rotation following surgery (p<
0.0001). Return of movement and strength decreased with increasing tear size. At the latest follow-up results were rated as excellent in 68 shoulders, satisfactory in 12, and unsatisfactory in 25. 8 out of the 11 massive tears had unsatisfactory outcome. There were
Standard tendon repair techniques combined with adequate postoperative protection and monitored physical therapy produced consistently satisfactory results. Introduction of experimental repair methods should be confined to those patients with massive tendon tears and only then with the hope of increasing function, as pain relief is satisfactory with usual treatment methods.
Arthroscopic acromioplasty is said to be a difficult procedure to learn although Gartsman stated that most surgeons can reliably perform an arthroscopic decompression after instruction in 10–20 cases. We assessed the learning curve for one consultant surgeon.Patients were selected on the basis of clinical examination and all had signs of impingement at arthroscopy. Surgery was performed between February 1993 and June 1996. Patients with full thickness tears were excluded from the study. The senior author had not performed any arthroscopic acromioplasties prior to providing a service in this hospital. Each shoulder was assessed immediately prior to surgery and at follow up using the Constant and Murley method of functional assessment without the power component. Patients were asked if they would have the operation again, with the benefit of hindsight.Of 89 shoulders complete preoperative and postoperative scoring beyond 6 months was available in 71. Of these, 62 operations were performed by one consultant (ANS) and 9 by trainees under his guidance. Patient questionnaires were completed for 73 of 89 shoulders.
A standard operative technique under general anaesthesia was used for all patients.
The overall improvement in shoulder function was 10.3 (SD 12.4) points (p< 0.0001). The change in shoulder score did not vary with increasing surgical experience. The length of operation, however, shortened with increasing experience with a mean of 106 minutes and 60 minutes for the first and last five operations. Questionnaire analysis found 82% would have the operation again.
In our study operative time reached a plateau after approximately the first twenty five cases but the results of these early operations are good.
The aim of this study was to review the effectiveness of percutaneous release of the common extensor origin for tennis elbow. The operative technique is similar to that previously reported by Hohmann in 1949.
There were 29 patients (31 elbows) that underwent the procedure between 1991 and 1998. There were 14 males and 15 females; 19 were right handed, and 17 had the dominant arm involved. The mean age was 51.8 years (range 34–65); the mean duration of symptoms was 21.7 months (range 8–60 months). All patients had a minimum of 12 months of conservative treatment including NSAIDs, splinting, physical therapy and local anaesthetic and steroid injections (2–6 injections). All operations were performed as day case procedures, with the majority (25) done under local anaesthetic. 24 patients were independently reviewed using Hospital for Special Surgery Elbow Assessment and a questionnaire. Grip strength measurements were performed using JAMAR Dynanometer and the level of patient satisfaction was recorded.
5 patients could not attend the special review clinics. They were contacted over the phone and necessary data recorded. The mean follow up was 45.2 months (range 8–88 months). 24 patients scored above 70 points and were very satisfied, 6 patients were considered failures as their symptoms warranted formal open release operation; only two reported an improvement following the open releases, with the remainder still symptomatic at the last follow up. An overall success rate of 81% was recorded. Complications were rare - one patient who had bruising of forearm after the procedure.
In conclusion this procedure can be recommened as an efficacious first line of surgical treatment, with advantages of being safe, quick to perform and with minimal morbidity.
Lumbar Degenerative Kyphosis (LDK) is a clinical entity showing kyphosis in the lumbar spine in elderly with multilevel disc narrowing and a varied degree of osteoporosis. LDK patient complains of stooped gait with persistent low back pain and weakness. Purpose of this paper is to study the lumbar muscle in LDK patients with histopathologic and biophysical evaluations to investigate the pathogenesis.
Materials and Methods: 1. Intramuscular pressure (IMP) (a) of the lumbar extensor compartment and hemoglobin content (Hb)□@(b) of 25 young volunteers were also investigated comparing in standing upright and flexion positions using (a)□@pressure monitoring kits and an non-invasive oxygenation monitor. 2.Muscle biopsy specimens obtained from the lumbar extensors of 9 LDK patients were histopathologically examined with HE, cytochrome c oxidase and other methods. These data were compared with muscles taken from age-match controls. Mitochondria function was also examined on biochemistry.
1. IMP of the extensors markedly increased in the flexion position (130.0□}45.4 in males and 86.3 mmHg in fem.) comparing to straight upright□@(22.8□}14.4, 17.0□}6.0). Oxy-Hb concentration decreased from 100% to 92.9, 95.5 % respectively in flexion, which was a sign of ischemia. 2. Both multifidus and sacrospinalis m. showed moderate to marked interstitial fibrosis, decreased number of muscle fibers and decreased stain intensity of cytochrome c oxidase. These finding were similar to those seen in repeatedly compressed muscles of an animal model of the chronic compartment syndrome. In comparison the rectus abd. and psoas muscles in the patients showed almost normal except for some aging changes. Conclusion: There appeared to be definite atrophy of the lumbar extensor muscles with histochemical and biochemical methods in LDK patients, whereas the flexors showed no change. This extensor atrophy is limited in the lumbar region in LDK. These localized atrophy of the lumbar extensors would suggest a result of high IMP during working in deep bending position of the spine for many years and may play important role in etiology of this disease condition.
This paper reports two studies of uncemented (UC) shoulder arthroplasty – one directed at UC humeral stems (Study 1) and the second at UC glenoid components (Study 2).
In Study 1, 160 consecutive UC humeral stems were inserted between 1989 and 1995. Three types of stem were used – Biomodular, modified Biomodular and Nottingham. At a mean follow-up of 4.3 years 18 shoulders were lost to follow-up. Of the remaining 142 shoulders radiographs from routine follow-up appointments at 6 months,1,2,3,5,7 & 9 years were reviewed together with a clinical follow-up of the patients.
In Study 2 a survival analysis was carried out on a consecutive series of 222 UC glenoid components inserted between 1989 and 1998 at a mean follow-up of over 5 years. Survival was defined as a prosthesis remaining in situ in a live patient. Six types of UC glenoid component were used – Copeland/Zimmer(non HA), stndard Biomodular, low-profile Biomodular, Nottingham prototype, Nottingham and Nottingham with HA.
In Study 1, radiological follow-up indicated 3 stems(2%) showed definite loosening (all related to deep infection) – all were revised. Six stems (4%) showed probable loosening but were asymptomatic.
In Study 2, for the whole series a survival table was created which identified a survival at 2; 5 and 10 years respectively of 92%; 75% and 66%. The later prosthesis designs performed best. A radiological analysis of all shoulders is currently in progress. This audit of outcome has indicated that hydroxyapatite has been beneficial but further long-term studies are required.
100 pre-operative and post-operative knee and function scores were analysed to assess whether a low pre-operative score was related to a poorer outcome, ie, are we operating too late? A two tailed student “t” test was performed showing that a pre-operative “function “ score of less than 30, resulted in a lower post-operative “function” score and the difference was statistically significant. These patients also showed the greatest improvement in scores and were the most satisfied with surgery. However, a low pre-operative “knee” score could not be related to a low post-operative “knee” score. Patients who had either a “knee” or “function” score of greater than 60 made no statistically significant improvement in either score. In conclusion, the pre-operative “knee” score is not a reliable indicator for when to perform surgery. However, the “pre-operative “ function score should be given more credence, along with clinical judgement, as it would appear that operating too late adversely affects the functional outcome of total knee arthroplasty.
The aim of this study was to evaluate the morbidity associated with carpal tunnel syndrome and the outcome following surgical treatment using the Nottingham Health Profile (NHP).
Between 1994 and 1996 we performed a prospective study of the effect of carpal tunnel release on the health status of 96 patients. The Nottingham Health Profile, a validated generic scoring system was used to assess quality of life, before and after surgery.
96 patients with 103 symptomatic hands were studied over this two year period. The patients completed a questionnaire before and 4 months after surgery. The notes were reviewed by an independent assessor and data collected with regard to duration and nature of symptoms, associated conditions, patients’ satisfaction and complications.
72 patients were satisfied with the results of surgery and 24patients were dissatisfied despite in the main clinical improvement. There was a significant improvement in the scores for pain, physical mobility and sleep 4 months following surgery in all patients.
We observed that those patients with a significantly high pre-op NHP score fared less well than cohorts, developing more frequent complications and overall were more likely to be dissatisfied with the results of surgery. This group of dissatisfied patients had previously been indistinguishable from their cohorts and were as it were invisible. The high NHP scores provided an objective way of identifying this group of individuals.
Carpal tunnel syndrome had a notable impact on the health status of our patients. There was a significant improvement in the NHP scores 4 months following surgery.
Our findings show that outcome assessment tools have predictive value in identifying patients who may not benefit from surgery or in whom a poor result might be anticipated.
The application of arthroscopic procedure for osteoarthritic knee is limited to rather initial stages of the disease. Here we report the results of new arthroscopic procedure, which was named arthroscopic posteromedial release, applied to relatively severe cases of medial type osteoarthrits (OA)
Forty-eight knees of 46 patients of OA knees with flexion contracture were treated with arthroscopic posteromedial release. Thirty-two were female and 14 were male. All the patients had been treated conservatively beforehand. The mean age of the patients was 71.6 (range, 47 to 84 years), the average range of motion was 13 to 129 degrees. Only one case was classified stage II in Kellgren Lowrence x-ray classification, 13 and 34 cases were stage III and IV respectively. The average femoro-tibial angle was 183.4+-4.4 degrees.
In surgery, we release the joint capsule along with the medial tibial condyle, arthroscopic debridement including medial meniscentomy was performed at the same time. If some cases, medial collateral ligament was cut transversely to obtain enough joint space. We use hyaluronan intra-articularly once a week for 5 weeks postoperatively. Patients were examined at 3,6,12,18 and 24 months after surgery and evaluated subjectively and objectively with the rating system of Japanese Orthopaedic Association knee score (JOA score). Clinical results were also classified excelletn, good, fair and poor by our criteria.
Eighty-three per cent (40 knees) of patients were satisfied at their last follow up. Sixty-seven percent (32 knees) of the patients were excellent or good. Six knees were converted to TKA because of their persistent knee pain. Twenty-eight knees complained of night pain pre-operatively, but only four of them complained of it postoperatively
Considering that most of the patients in this series were grade IV in x-rays and their joint surface of medial compartment showed large eburnation both femur and tibia, TKA is most preferable treatment conventionally. But our results showed this arthroscopic technique was one of the applicable choices for severe OA knees.
65 patients over the age of 80 years, who underwent a total knee arthroplasty between 1989 and 1994, were retrospectively reviewed, by means of questionnaire, phone call, clinical and radiological examination.Notes were reviewed for pre-existing medical conditions, pre-operative and post-operative Knee Society “Knee” and “Function” scores. They were then compared with 65 randomly selected patients in a different age group, 70 years and under.56 octogenarians were alive at 5 years and 50 available for full review.
Elderly patients had more pre-existing medical conditions, with hypertension a ubiquitous diagnosis, required a longer in patient stay and more social services input before discharge, than the younger age groups. All patients in the elderly group suffered from osteoarthritis, unlike the younger age groups. Valgus deformity of the knees was only seen in the younger cohort. Previous surgery was more common in the octogenarians, with more octogenarians having undergone a tibial osteotomy and more youngsters undergoing arthroscopy. A reflection of changing surgical practice.
“Knee” Scores were not significantly different between the age groups. However, the “function “ scores pre-operatively, were significantly lower in the over 80s and they made a more significant post-operative gain. Post-operatively, elderly male patients were more likely to go into retention post-operatively, than female patients and males in the younger age group.
None of the prostheses had required revision in the elderly age group and only 5 patients had died since the surgery. None of the deaths were related to the surgery.
We recommend pre-operative catheterisation of octogenarian patients, especially those with a history of prostatism. There would appear to be from this review no indication for denying elderly patients an arthroplasty on the basis of age.
To assess total knee arthroplasty function in osteoarthritic patients who had their arthroplasty aged 55 years or less.
Self administered questionnaires were posted to 150 patients who had been registered on the Trent Regional Arthroplasty Register as having their TKA for osteoarthritis aged 55 or less. 85% of questionnaires were returned completed giving us information on 136 TKAs. The mean age of the patients at TKA was 51 yrs (Range 29 – 55 yrs.). Male 60: 67 Female. The mean follow-up was 44 months.
41% of patients had had no knee surgery prior to their TKA. 9 had had a corrective osteotomy.
51 patients had to give up work because of their osteoarthritic knee, only 17 got back to work after their TKA. 80% of patients felt that their arthroplasty had met or exceeded their pre-operative expectation in relieving pain though 41% continue to experience moderate or severe knee pain and 29% continue to have regular night pain. 62% of patients felt that they had been able to resume leisure activities to the same or better level than expected pre-operatively.
Volar wrist ganglion has a different mode of origin and higher complication rate after excision compared to its dorsal counterpart. This study, which is part of the Trent region ganglion audit, was carried out to prospectively evaluate the natural history and treatment outcome for volar wrist ganglia.
Patients were invited to join the study between 1993 and 1995 following initial consultation with either an orthopaedic or plastic surgeon. Questionnaires were sent within the first year, at two years and finally at five to six years. The final review included a Patient Evaluation Measure (PEM) questionnaire.
Of the 234 patients initially consulted, 186 joined the study, 155 of these responded, 122 at final review and 109 at year two. There were 98 females and 57 males. Three patient groups were identified:
Group I: natural history (no intervention) (N=38)
Group II: aspiration/injection (39)
Group III: excision group (78)
In conclusion, over half of volar wrist ganglia disappear without any intervention between 2 to 5 years. About 45% recur whether aspirated or excised. There is a 18% complication rate with excision, but neither aspiration/injection nor leaving them alone with reassurance was associated with any complications. Irrespective of the treatment, about 80% of patients are satisfied at five years, slightly more than at two years.
This information may form a basis for patient information before deciding treatment. It could also help general practitioners advise patients before hospital referral.
Increasing emphasis is placed on outcomes research. In this community study knee outcomes scores were evaluated in a ‘normal’ elderly population
The American knee society (AKS), Oxford, and Bristol knee scores were recorded in 100 elderly people without a history of lower limb disorder. The mean age of subjects was 72 years. Mean normalised scores were 90%, 91% and 94% for AKS, Oxford and Bristol knee scores respectively. There were significant negative correlations between knee score and advanced age (p< 0.001) and knee score and co-existent major medical disorders (p< 0.001). The function component was the score component most senitive to these variables (p< 0.001)
Control studies are necessary if knee scores are to be taken as accurate measures of outcome. Comparison of outcome after knee replacement on the basis of knee scores should take account of demographic variables. Scores with a large ‘function’ component appear to be more susceptible to demographic variation.
Between 1982 and 2000, 37 cases of fractures of the odontoid process were treated at Hirosaki University Hospital. There were 16 females and 21 males, with an average age of 43.9 and 37.7 respectively. Twenty-three of 37 were type II and 14 were type III by the classification of Anderson and D’Alonzo. Eight of type II were old fractures. Nineteen of them were injured in traffic accidents, 9 in accidental falls from a height, 4 by falling down, 2 in lumbering accidents and 3 by unknown causes. Severe neurological disorders were recognized in 7, mild in 12 and 22 had no neurological disorders. Neurological disorders were correlated with SAC (space available for spinal cord) at C1-2. Twenty-two of type II (95.7%) and 10 of type III (71%) were treated surgically. Surgical methods were anterior screw fixation of the odontoid process in 7, anterior atlanto-axial joint fixation in 3, posterior atlanto-axial joint fixation in 5, posterior occipito-cervical fusion in 3, anterior and posterior combined fixation of the atlanto-axial joint in 2 and others in 2. Bone union was obtained in 18 (81.8%) of type II and 10 (100%) of type III by the primary operations. There was no nonunion in anterior screw fixation cases. Nonunion occured in one of type II (100%) and 2 of type III (50%) treated nonoperatively. Two of them were operated for nonunion. One of them remained nonunion by two additional operations. No case of nonunion showed neurological deterioration for 91.8 months after treatment on average. Anterior direct screw fixation of the odontoid process is superior to the other methods in the point of immobilization of the odontoid fragment without limiting the motion of the atlanto-axial joint. We recommend anterior direct screw fixation of the odontoid process as a first choice of the surgical method for fresh fractures of the odontoid process in cases with reduced fragments.
Signal intensity changes of the spinal cord on MRI in chronic cervical myelopathy are thought to be indicative of the prognosis. However, the prognostic significance of signal intensity change remains controversial.
The purpose of this study was to investigate the characteristics of MR findings in cervical compression myelopathy that reflect the clinical symptoms and the prognosis and to determine the radiographical and clinical factors that correlate to the prognosis.
The subjects were 73 patients who underwent cervical expansive laminoplasty. Their mean age was 64 years, and the mean postoperative follow-up was 3.4 years. The pathological conditions were cervical spondylotic myelopathy in 42 and ossification of the posterior longitudinal ligament in 31.MRI (spin-echo sequence) was performed in all patients. Three patterns of spinal cord signal intensity changes on T1-weighted sequences/T2-weighted sequences were detected as follows: normal/ normal.
(N/N); normal/ high signal intensity changes (N/Hi); and low signal intensity changes/high signal intensity changes (Lo/Hi). Surgical outcomes were compared among these three groups. The most useful combination of parameters for predicting prognosis was determined.
There were 2 patients with N/N, 67 with N/Hi and 4 with Lo/Hi signal change patterns before surgery. Regarding postoperative recovery, the preoperative Lo/Hi group was significantly inferior to the preoperative N/Hi group. The best combination of predictors for surgical outcomes included age, preoperative signal pattern and duration of symptoms.
The low signal intensity changes on T1-weighted sequences indicated a poor prognosis. We speculate that high signal intensity changes on T2-weighted images include a broad spectrum of compressive myelomalacid pathologies and reflect a broad spectrum of recuperative potentials of the spinal cord. Predictors for surgical outcomes are preoperative signal intensity change pattern of the spinal cord on radiological evaluations, age at the time of surgery and chronicity of the disease.
The Bristol Knee Replacement Registry was established in the 1970’s and contains prospectively recorded data on 3024 patients. The present study examines the group of 812 patients for whom complete pre-operative and five year post-operative data is available in order to relate their eventual health status to the pre-operative demographic data and to disease severity. The group comprised 593 women and 219 men who had undergone either Kinematic, Total or Sled unicompartmental knee replacement.
Pre-operatively, the average American Knee Society Score (AKSS) was 89 with the elderly, rheumatoid patients and women having significantly lower scores.
Five years later the average AKSS had risen to 161 with patients of all ages, (including the over 80’s) gaining considerably. However, the rheumatoid patients remained more disabled as did women who had a final AKSS of 157 as opposed to 171 for the men (p< 0.01). In addition, a statistically significant finding was that those with the lowest pre-operative scores also had the lowest 5 year scores - they never catch up.
173 patients underwent bilateral knee replacement at separate times. Their pre-operative AKSS was significantly higher at the time of the second knee replacement (90) than the first (82) p< 0.01.
We conclude that since patients present earlier for their second TKR and those with most disability fail to catch up the procedure should be performed earlier in the natural history of the disease, especially in women.
In currently used expansive laminoplasty (ELAP) for cervical spondylotic myelopathy (CSM), persistent axial pain, restriction of neck motion and loss of cervical l ordosis have been the significance postoperative problems. To prevent them, the author has developed skip laminectomy in which ordinary laminectomy at appropriate levels is combined with partial laminectomy of the cephalad half of laminae with preservation of the muscular attachments at adjacent levels. Since December 98, the author performed this procedure on 55 patients with CSM who required multilevel posterior decompressions. Twenty-one of these cases with follow-up period longer than 8 months, with an average of 12 months, were observed.
In skip laminectomy, a consecutive four-level decompression between C3/4 and C6/7 as an example is accomplished by removing alternate laminae (C4 and C6), the cephalad half of the C5 and C7 lamina and the ligamentum flava at those four levels. The laminae to be removed were selected after analysis of the pre- and postoperative radiological findings.
Intraoperative blood loss averaged 34 grams. The operation time averaged 128 minutes. The patients were allowed to sit up or walk on the first postoperative day without neck support of any kind. An average recovery rate according to the Japanese Orthopaedic Association score was 63%. None of these patients complained of residual axial pain. The postoperative ranges of neck motion on lateral X rays averaged 87% of the preoperative ranges. The spinal curvature index, according to Ishihara’s method, was reduced in only one of the 21 cases. Postoperative atrophy of the deep extensor muscles measured on T2 weighed axial MRI was minimal.
Skip laminectomy is less damaging to the posterior extensor muscles and its use reduces the postoperative problems commonly seen after ELAP.
Craniovertebral tuberculosis accounts for 5% of all cases of tuberculosis and is the commonest infective pathology affecting this region. There are very few published reports discussing the presentation and management of this complex pathology.
30 cases of craniovertrebral tuberculosis treated between 1989–97 were reviewed retrospectively. The average age was 24 years (range 6 – 42 years) with a follow up of 41 months (range 36 – 48 months). Two main groups on the basis of atlantoaxial stability. 18 (60%) had an unstable atlantoaxial articulation and of these 12 (66%) had a fully reducible AAD in extension. 17 patients (56%) had varying degrees of neurological deficit with lower limb spasticity being the commonest.
Antituberculous chemotherapy, skeletal traction in extension and prolonged bracing with moulded philadelphia collar were main stays of conservative treatment. Surgery in the form of posterior occipito cervical arthrodesis was needed in 13 patients (43%) and indications included incompletely reduced AAD, non resolving neurological deficit and persistent instability despite 6 weeks in traction.
There was 93% success rate with resolution of infection (range 4 – 8 months) and improvement in neurological deficit 2 patients had incomplete neurological recovery and required 2nd stage anterior transoral odontoidectomy. Management strategies based on the presence or absence of instability and neurological deficit can give a very satisfactory outcome with judicious combination of drug therapy, bracing and surgical decompression with fusion.
All types of cervical laminoplasties for cervical spondylotic myelopathy (CSM) gave the same degree of postoperative neurological recoveries. However, postoperative neck functions differed according to degrees of intervention with posterior supporting elements of the neck (spinoligamentous complex, SLC). To obtain optimal postoperative neck function, SLC should be preserved. Laminar enlargement destroying SLC resulted in anterior tilt of neck, loss of cervical lordosis and loss of cervical range of motion (ROM) by 40–60% of preoperative ROM, whereas, tension-band laminoplasty (
To obtain optimal postoperative neurological recovery, the timing of decompression was a key issue. Japanese Orthopaedic Association (JOA) score for cervical myelopathy (normal = 17 points) was used for neurological evaluation. One hundred and nine patients who underwent tension-band laminoplasty, were grouped into 3 groups according to preoperative JOA scores: group A with JOA score above 14 (10 patients), group B with JOA score between 11 and 13 (48 patients), and group C with JOA score below 10 (51 patients). Mean pre-/post- JOA scores and ratios of patients with postoperative JOA score above 16 for each group were as follows: 1
0.4/14.1, 34% for total patients, 14.6/16.5, 80% for group A, 11.9/14.8, 40% for group B, and 8.2/12.9, 20% for group C. There was a statistical difference among three groups.
It was concluded that decompression at the early stage with JOA score above 14 using tension-band laminoplasty might provide the best outcome to CSM-patients regarding neurological improvement and postoperative neck function.
An acute phase of periprosthetic bone loss occurs following total hip arthroplasty (THA). Periprosthetic bone loss undermines implant support, may contribute to its failure, and complicates revision surgery as allograft may be required to replace lost bone. We assessed the effect of a single 90mg dose of the bisphosphonate pamidronate on early periprosthetic bone mineral density (BMD), biochemical markers of bone turnover, and clinical outcome in 47 men and women undergoing hybrid THA in a randomised, double-blinded, placebo-controlled trial.
The mean (± 95% CI) differences in BMD (area under BMD change.time curve) between those receiving pamidronate and those receiving placebo was 0.91(± 0.51) g.weeks/cm2 for the proximal femur (P=0.002), and 0.80 (±0.60) g.weeks/cm2 for the pelvis (P=0.009). Patients in the pamidronate group had suppression of all biochemical markers of bone turnover compared to placebo (P< 0.05), except for urinary free deoxypyridinoline. Both treatment groups experienced similar improvement in Harris hip and SF-36 UK outcome scores. The frequency of adverse events was similar in each treatment group (placebo 7/24, pamidronate 8/23, P> 0.05).
Acute periprosthetic bone loss following THA is due to a transient increase in bone turnover. A single dose infusion of pamidronate in the early post-operative period significantly reduces this bone loss, and is well tolerated.
The results of 278 consecutive primary total hip arthroplasties performed with bone grafting for ace-tabular bone deficiencies were reviewed at an average of 9.0 years (range, 5–23) after surgery. All patients had underlying developmental dysplasia of the hip. For all hips, the grafts used were from the patients’ own resected femoral heads. All but three grafts were screwed to the supero-lateral aspect of the acetabular roof, the exceptions being grafts without internal fixation. Kaplan-Meier survivorship analysis predicted a rate of survival of the acetabular component at 10 years of 97% (95% confidence interval (CI), 94–100%) with revision for aseptic loosening as the endpoint, and of 82% (95% CI, 76–89%), when radiological loosening was used. Trabecular reorientation, as an indicator of graft incorporation, was seen in 89% of the joints between 1.5 and 5 years (mean 3 years), and delayed up to 7 years. Parametric survivorship analysis using the Cox proportional-hazards model indicated that trochanteric non-union, lateral placement of the socket, and delayed trabecular re-orientation of the bone graft, were risk factors for loosening of the acetabular component. Autogenous acetabular bone grafting will be of value for long-term success and has good potential for additional improvement of the results, provided these three risk factors are reduced. In order to promote the trabecular reorientation, we have gradually improved the surgical technique including sizing of bone graft and adaptation technique. By these alterations of the surgical technique, trabecular reorientation of the 51 joints operated after 1993 was completed by 4 years after surgery.
To establish whether there were features present on the initial post-operative radiographs of total hip replacements (THR) predictive of aseptic loosening.
Our data was derived from the Trent Regional Arthroplasty Study (TRAS) which is the only hip register of its kind in the country. The TRAS commenced in 1990 and has recorded clinical and operative details of all THRs in the region.
Our current study was concerned with a cohort of grossly loose THRs, identified from the five-year follow up of those patients who had undergone THR in 1990. Our cohort are those which failed specifically due to aseptic loosening and comprises those revised or listed for revision as well as a number of previously undiagnosed cases.
The post-operative radiographs were analysed, recording the following: (1) number, width and location (Gruen zone) of radiolucencies at both cement-bone and cement-prosthesis interfaces; (2) presence of stem-cortex contact; (3) width of the cement mantle in each Gruen zone; and (4) Barrack cementation grade.
Occasionally, if the initial post-operative radiograph was of poor quality, then further information was gained from the next available ones (usually at six weeks) to improve accuracy.
Comparisons were made with 60 control hips randomly generated from the same 1990 cohort but which had not failed.
Chi-squared tests were used to test the probability of obtaining the observed data by chance and odds ratios were calculated to describe relative risk of failure for different risk factors.
Hips with inadequate cementation grades (C and D) had a 9.5 times greater risk of failure compared to those with adequate cementation grades (A and B) [p< 0.0001].
We have demonstrated that the grade of cementation has a major effect on the probability of failure. This emphasises the importance of good cementing, which is particularly relevant in this era of clinical governance where there is greater accountability on the surgeon for adequate performance.
Total hip arthroplasty surgery may be associated with substantial loss of blood often necessitating blood transfusion.
The risks associated with blood transfusions are widely known. Haemostatic drugs have been tried in the past to try and reduce this, and there has been renewed interest in these recently, in particular Aprotinin (Bayer).
Aprotinin is a serine protease inhibitor, which has been shown to reduce blood loss in cardiac surgery by up to eighty percent.
The aim of our study was to investigate whether or not high dose Aprotinin can reduce blood loss and transfusion rates in patients’ undergoing total hip arthroplasty.
This was a randomised double blind controlled clinical trial, where 50 patients were randomised to receive either Aprotinin (2 x 106 KIU followed by an infusion of 5 x 105 KIU/hr), or an equivalent volume of normal saline.
Blood loss and transfusion rates were measured as well as the incidence of deep vein thrombosis.
There was a significant reduction in total blood loss seen in the Aprotinin group, median 817±350, when compared to the control group, median 1191±386. This translates to a 31% reduction in blood loss.
DVT and transfusion rates were not significantly different between the two groups.
There was no complications or deaths seen in the Aprotinin group.
The use of high dose Aprotinin results in a reduction in blood loss in total hip arthroplasty. It has been proved to reduce blood loss in cardiac surgery, and although papers have shown it can reduce blood loss in orthopaedic surgery, its’ use should not as yet be routine.
Further work is required to investigate the possibility of a future role for Aprotinin in orthopaedic surgery, as well as its’ mode of action. Until then more established methods of blood conservation should be used.
The Charnley total hip replacement has had favourable long-term survival results. On the strength of these results orthopaedic companies have introduced “Charnley Copies” incorporating identical design parameters.
The objective of the study was to determine whether the acetabular cups provided as DePuy Charnley copies by different manufacturers are identical with regards to their geometry. To analyze how any differences present may affect the motion characteristics of the arthroplasty.
A jig was designed which allowed the measurements of: i) range of movement free from impingement, ii) the arc of movement during which the femoral neck is impinging on the cup, iii) point of subluxation and dislocation of the femoral head from the cup. The cups obtained for analysis where the Standard and Long Posterior Wall models of the DePuy Charnley, Aesculap ALFA, Corin Cenator and Avatar LFA. The Aesculap Plasma Symmetrical and Asymmetrical were analyzed for comparison.
The Alfa has a greater free range of movement compared to the Charnley cup and the other copies. The Charnley cup, the Cenator and the LFA differed in their pattern of impingement. The Alfa had the earliest point of dislocation. Long Posterior Wall: The Avatar had the greatest free ROM. The Charnley and the Alfa dislocated in an anterior direction latest. The Avatar and Cenator dislocated latest in the posterior direction. Plasma Cup: Compared to the Charnley and its copies its free range of movement was greater, it had only one point of impingement and impinged through the smallest arc before dislocating. It did, however, dislocate easiest.
Charnley copies are not identical. Differences in geometry exist and these alter important motion characteristics. Long term outcome may be affected. Surgeons should be aware of these differences when choosing implants.
To clarify the short-term results of conservative treatment for symptomatic full-thickness tears of the rotator cuff.
Between September 1996 and August 1999, 107 shoulders of 105 patients were diagnosed as full-thickness tears of the rotator cuff by MRI or arthrography at our institute. All patients were treated conservatively and only 3 shoulders underwent surgery because of persistent pain after 6 months of conservative treatment. Among 104 shoulders treated conservatively for more than 12 months, 102 shoulders of 100 patients were followed up with an average follow-up period of 33 months. Two patients were excluded: one had died and the other had been lost at the time of follow up. Among 102 shoulders, 56 shoulders of 56 patients were assessed by direct examination, and 44 shoulders of 46 patients were interviewed by telephone. There were 54 males and 46 females with an average of 64 years (44–80). The Shoulder Functional Evaluation by the Japanese Orthopaedic Association (JOA score) was used for assessment (full score = 75 points)
The overall JOA score improved significantly from 41.3 points (initial) to 63.5 points (follow-up) (p< .01). Satisfactory results (> - 60 points) were obtained in 71%. The pain score (full score = 30 points) improved from 8.3 points (initial) to 24.7 points (follow-up) (p< .01). At follow-up, 49% had no pain and 88% did not need any medication. The range of motion, abduction strength, and activities of daily living improved significantly (p< .01). Angle of external rotation at initial examination was positively correlated with the JOA score at follow-up (r=0.373, p> .01).
Short-term outcome of conservative treatment for symptomatic full-thickness tears of the rotator cuff was satisfactory in 71% of the patients.
A powered, randomised control trial was instigated to evaluate the advantages of subacromial injection of Methylprednisolone over conservative treatment in the management of partial rotator cuff injuries of the shoulder.
Consecutive patients with possible partial rotator cuff tears were reviewed at 1 week. Inclusion criteria for a diagnosis of partial rotator cuff tear included; traumatic mechanism, greater tuberosity tenderness, painful arc, and complete resolution of disability post-Bupivicaine block. Exclusion criteria included; age < 16 years, chronic shoulder disease, acromioclavicular tenderness, and abnormal shoulder radiograph. Patients were randomly allocated to receive either 1 immediate subacromial injection of 40mg Methylprednisolone (group S) or no injection (group N). Initial outcomes measured were; visual analogue pain score (0–10) and active abduction (nearest 5°), repeated at 3, 6, and 12 weeks. All patients were instructed in analgesia usage and given identical shoulder exercises.
Of 279 patients reviewed over 3 years, 90 met the inclusion criteria (6/90 patients were lost to follow-up). 50 patients were randomised to group S, 40 to group N. Mean pain score improvement at 12 weeks was comparable (S=4.95, N=4.44) (p> 0.1, CI=0.16–0.86). In patients aged > 40 years group S had significantly higher mean improvement in abduction at completion (64.28°) compared to group N (34.63°) (p< 0.02, CI 1.29–58.01). Conversely in patients aged < 40 years group S had lower mean improvements in abduction (40.55°) compared to group N (77.73°), though this was not statistically significant (p=0.1, CI 2.06–72.29)
Methylprednisolone injection is more efficacious than conservative treatment alone in some patients. This benefit appears age-dependent and consequently such treatment should be reserved for patients aged > 40 years.
This study was performed to assess the relationship between patients’ pre-operative symptoms and their expectations at the time of revision hip arthroplasty. The WOMAC (Western Ontario and McMaster Osteoarthritis Index) scale for osteoarthritis of the hip and the Short Form 36 (SF-36) general health status scale have both been validated for the assessment of the outcome of hip arthroplasty. We prospectively assessed 60 patients using these scales as well as the “expectation WOMAC” that asked the patients to estimate how they expected to feel 6 months after revision hip replacement. All the questions were completed prior to informed consent, and were scored form 1 to 5 with increasing severity with a Likert scale. The maximum possible scores for pain, stiffness and difficulty with physical activity were therefore 25, 10 and 85 respectively.
The mean preoperative WOMAC score for pain was 13.4 (CI 12.2.-14.6), for stiffness 5.9 (CI 5.6-6.2) and for physical activity 50.9 (CI 47.2-54.6) The mean expectation WOMAC scores for these modalities were 7.4 (CI 6.2-8.6), 3.5 (CI 3.0-4.0) and 28.1 (CI 24.0-32.2.) respectively. Although there was a wide spread of expectations, we were unable to find any significant correlation between the patients’ preoperative pain and The abstracts were prepared by Mr Simon Donell. Correspondence should be addressed to him at the Department of Orthopaedics, Norfolk & Norwich Hospital, Level 4, Centre Block, Colney Lane, Norwich NR4 7UY, United Kingdom. stiffness levels and their expectations for pain and stiffness after revision hip arthroplasty. There was however a statistical association between their preoperative difficulty with physical activity and their expectations for physical activity (r=0.38; p=0.02) There was no significant correlation between the SF-36 scores and the patients’ expectations.
The expectations of patients awaiting revision hip replacements are high, and do not appear to be closely related to their level of pre-operative disability. Even patients with severe symptoms have high expectations that in some cases may be unrealistic. The use of the “expectation WOMAC” may help us to identify such patients, and to improve patient education and satisfaction.
A modified Kessel trans-acromial approach has been utilised in our Unit for decompression and repair of associated rotator cuff tear for all advanced impingement syndrome (Stage III). This preliminary report aims to review our results, and to assess the complications of this approach.
From 1996 to 1999, 22 consecutive patients who were treated surgically using a Trans-acromial approach for advanced impingement syndrome, were reviewed. The diagnosis of impingement syndrome was based on history, physical examination and Lignocaine impingement test, with either an ultrasound scan, arthrogram, or MRI. The modified trans-acromial approach was used involving splitting and raising a periosteal soft tissue flap over the acromion, followed by splitting the acromion in the coronal plane just behind the acromioclavicular joint, this allowed an extensive exposure of the rotator cuff and easy undercutting of the acromion.
20 patients were interviewed and examined specifically for this study, for an average follow up of 17 months. The other two patients were interviewed by telephone. The following parameters were studied: 1) functional assessment:[Constant’s Scoring system, and the UCLA Shoulder rating Scale. 2) Pain relief. 3) Patient satisfaction. 5) Return to preoperative activity. 6) Complication. The results were satisfactory in 17 patients (77%), and unsatisfactory in 5 pt (23%), one of which had cervical spondolysis, and two had new bony formation in the subacromial space. Pain relief was achieved in 78%. All patients returned to their preoperative occupation apart from one. Two patients had persisting impingement and had undergone revision subacromial decompression with satisfactory results.
The modified trans-acromial approach is an acceptable alternative to open anterior acromioplasty. It offers adequate decompression of the sub-acromial space, allowing a wide exposure and excellent visualisation of the rotator cuff. This facilitates cuff repair and mobilisation, while maintaining the integrity of the deltoid muscle, which accelerates postoperative rehabilitation.
At least 10% of consultations in General Practice are for musculoskeletal problems. It would seem appropriate that the diagnosis and management of common musculoskeletal problems should form an important part of the “core” curriculum of any undergraduate medical training. Time is always short in an undergraduate teaching program and the pressures not to overload the curriculum are constant. The planned increased in student numbers is likely to stretch the ability of most teaching departments to provide a high level of undergraduate training in musculoskeletal disease.
A postal survey of the provision of undergraduate teaching in T& O was performed in the UK. All 23 medical schools in England, Scotland, Wales and Northern Ireland were. To gain further insight into non-specialist general training in T& O after qualification a survey of the Vocational Training Schemes (VTS) for General practitioners in the Northern Deanery was performed.
Ninety-one percent of Medical Schools replied. The average length of the orthopaedic attachments (all years combined) was five weeks. However, all but two programs were combined with other clinical subjects. The dilutional effect of these other subjects resulted in the average duration of the T& O attachment being reduced to 2.7 weeks (range 1.5 – 6). All the modules in orthopaedic surgery except one included trauma within the curriculum.
There are four VTSs in the Northern Deanery. All of these had schemes that included A& E but not for every trainee. No scheme had either a rheumatology or orthopaedic surgery placement, although some exposure to rheumatology occurred during attachments in general medicine.
This study shows that there is a significant discrepancy between the amount of time, within the curriculum (4%), devoted to musculoskeletal/orthopaedic teaching and the number of consultations in General Practice (10%); this discrepancy is not made up during VTS placements. In addition, such short exposure to a large subject may encourage superficial learning which medical education is specifically trying to avoid.
We hypothesise that patients are unable to recall much of the information imparted during the informed consent procedure. This may have important medico-legal consequences and increase patient anxiety. Receiving the information in a written format may improve patient recall. There have been no previous studies testing recall or information sheets for British orthopaedic patients.
We performed a randomised controlled trial of consent for total hip arthroplasty, with one group of patients receiving a written information sheet with explanation as necessary, and the control group receiving the same information verbally. The consent was obtained at a pre-operative assessment clinic approximately three weeks before admission. On admission, a questionnaire was filled in both groups of patients to assess recall.
There were no significant differences between the two groups with regard to type of arthroplasty (revision or primary), age, or days from consent to admission.
The group receiving written information performed better in the recall questionnaire. This group were pleased to have received the information sheet, there were no negative comments about the sheet. In the group who received verbal information, most expressed a desire to receive a written information sheet. One patient stated that she would rather know nothing about the operation and would have refused a sheet. We conclude that patient information sheets are an acceptable and appropriate method of imparting the necessary information for informed consent for total hip arthroplasty, and are more effective than standard verbal informed consent.
Medico-legally, the sheet could be a permanent record of what was discussed. This should prevent disputes and claims due to poor recall of the consent procedure.
In Total Knee Arthroplasty (TKA) and Total Hip Arthroplasty (THA) the total blood loss is composed of ‘visible’ blood loss from the surgical field and wound drainage, and blood loss into the tissues which is ‘hidden’. Blood management should be aimed at addressing the total blood loss.
56 TKAs and 46 THAs were prospectively studied. TKAs were performed with tourniquet. After tourniquet release, all drained blood was salvaged and significant volumes reinfused. No reinfusion was used for THAs.
The true total blood loss was calculated in the following way:
Patient Blood Volume (PBV) is: [1]
PBV = k1 x height3 + k2 x weight + k3
Therefore patient total Red Blood Cell volume (RBCv) is:
RBCv = PBV x Hct. (where Hct is Haematocrit)
Total RBCv loss = PBV x (Hct preop – Hct postop) + ml RBC transfused
The result is reconverted to Whole Blood volume.
Hidden Loss = Total Loss – Visible Loss.
In TKA, the mean total true blood loss was 1474ml. The mean hidden loss was 735ml. Therefore hidden loss is 50% of the total loss and the total true loss following TKA is twice the visible volume. In THA, the mean total true blood loss was 1629ml. The mean hidden loss was 343ml.
Thus hidden loss in THA is much smaller. (21%) Total loss is 1.3 times the visible loss. In the TKA group, comparing patients with large losses receiving reinfusion and those with small losses not receiving reinfusion, the proportion of total true loss which was hidden was the same, at 50%.
Patients with Body Mass Index (BMI) > 30 were compared with those with a BMI < 30 and no correlation was found between BMI and Hidden Loss.
Joint Replacement Surgery involves a ‘hidden’ blood loss which is not revealed and cannot be measured or reinfused in practice, but which should be taken into account when planning blood loss management. In TKA it is substantial. In THA it is much smaller and probably not of as much clinical concern. Hidden loss is no greater in the Obese patient.
Skeletal tuberculosis is an indolent disease whose diagnosis is often delayed. Evidence of pulmonary tuberculosis is present in less than 50% of cases. We present our experience from a small inner city district hospital of the difficulties managing patients with skeletal tuberculosis.
During the period 1988 to 1998 a total of 38 patients with tuberculous osteomyelitis confirmed microbiologically by tissue culture or histologically on material gained at biopsy presented to our inner city hospital serving 250 000 patients.
Two groups of patients were identified in our series. There was an acute group that tended to affect the appendicular skeleton and who responded to local treatment plus chemotherapy with restoration of normal function. In contrast the second group, who were difficult to diagnose, had axial skeleton involvement, deteriorated before treatment and had a poor outcome despite treatment. Failure of admitting medical teams to examine the axial skeleton in their confused patients led to a delay in diagnosis of skeletal tuberculosis in this second group with profound consequences.
All health professionals will be encountering skeletal tuberculosis more frequently with the recent resurgence of pulmonary tuberculosis. They may have little experience with the management of this condition and may overlook the diagnosis with consequent catastrophic results. A high index of suspicion is required for prompt diagnosis with early referral to an orthopaedic surgeon improving outcome.
Survival in the wake of hindquarter amputation and oncological treatment is improving; the hindquarter amputee population is increasing. Some amputees function well others do not.
To assess quality of life and function of hindquarter amputees.
21 amputees (10 females and 11 males) consented to take part in the study. Ethics approval was sought. Assessment was performed using postal questionnaires; SF36 for quality of life; TESS (Toronto Extremity Salvage Score) for physical function and mobility; IEFF( International Index for Erectile Function) for male sexual function; a prosthetics questionnaire to assess prosthetic use.
Mean age of the group was 55 with the mean survival of 7 years post amputation.
Quality of life results were compared to normal subjects and patients for long tern illness. Amputees had a significant reduction in quality of life concerning physical function and pain. Social function, mental health and energy levels were equivalent to patients with long term illness.
The mean TESS result was 56.9 with females having a mean score of 61.7 and male of 48. 50% of the group considered themselves as severely to completely disabled; 50% considered themselves moderately disabled. Five were in full time employment.
Six males responded to the sexual function questionnaire. Impotence was universally experienced.
Only five amputees used their prosthesis regularly. All amputees have experienced and 20 continue to experience phantom pain.
This study illustrates that hindquarter amputees have poor physical function and a low quality of life. Phantom pain is universally experienced. Male amputees experience impotence. Addressing these areas would improve the life of current and future hindquarter amputees.
The latest government targets state that by the end of 2005 the maximum waiting time for an outpatient appointment will be 3 months. These recommendations will not only increase the size of the outpatient clinics, but also the resources required thereafter. The purpose of this study was to analyse the outcome of new knee referrals to one consultant’s knee outpatient service in order to quantify the resources required to investigate and treat these patients.
All new patients attending one consultant’s knee out-patient service in the time period January 1st 1997 to December 31st 1997 were prospectively entered into a database recording patient details, source of referral and provisional diagnosis.
Eighteen months after the time period a cohort of 200 patients was randomly selected and the notes were analysed retrospectively. The number of outpatient appointment episodes (OPAs), MRI scans, physiotherapy referrals and surgical episodes generated were recorded for each patient.
Analysis of the initial database records show that a total of 662 new knee referrals were seen in 1997. 52% (341) were made up of the five most common diagnoses, these being osteoarthritis, anterior knee pain, major anterior cruciate ligament injury, medial ligament injury and medial meniscus injury.
Retrospective analysis of the 200 patient notes revealed that these patients required a total of 511 OPAs, 38 MRI scans, 178 courses of physiotherapy and 93 surgical episodes (53 elective and 40 daycase/emergency). These figures can be extrapolated to account for the total number of patients seen:
The resource implications of a new knee referral are substantial. Extra resources must accompany each new patient, otherwise, although government targets will be reached the time taken to complete each patient’s treatment will become longer. It is imperative that before an agreement is made to see new patients the resources required to manage them are in place.
To investigate the incidence of complications arising from clavicle fractures in children and the need for multiple review in fracture clinic.
Retrospective analysis of 200 children with isolated clavicle fractures. The number of clinic visits was documented along with the mechanism of injury and any complications attributable to the fracture. Plain radiographs allowed classification of the fractures both in terms of site and type of fracture. Prospective analysis of 60 children with isolated clavicle fractures. All patients were discharged with a patient information sheet after their first fracture clinic appointment and were reviewed a minimum of 6 months post injury to assess clinical outcome/complications and patient satisfaction.
Retrospective review failed to provide any evidence of long term complications from isolated clavicle fractures. Two patients complained of a non-specific tingling in the arm which had settled within 2 weeks. No intervention other than rest in a broad arm sling was deemed necessary in any of the 200 children. Despite this, the average number of clinic appointments was 2.8.
In the prospective study there were no complications arising from an isolated clavicle fracture. Two patients returned (one at 6 weeks and one at 12 weeks) with concerns about the cosmetic appearance of the fracture site - both patients were reassured and discharged. All patients were satisfied with the cosmetic appearance and function of their shoulder when reviewed at a mean of 7.3 months post injury (range 6–10 months). All patients and/or guardians were satisfied with the patient information sheet.
Isolated clavicle fractures in children are rarely complicated by injuries such as skin necrosis or a neuro-vascular deficit. Despite this, children are commonly reviewed many times by juniors in a busy fracture clinic. We suggest that such review is unnecessary and that uncomplicated fractures may be safely discharged with a patient information sheet after the first clinic appointment.
The displaced intracapsular fracture in the elderly has frequently been termed the ‘unsolved’ fracture because of the debate as whether the femoral head should be preserved or replaced. To answer this question 413 patients aged over 70 years with a displaced intracapsular fracture were entered into a prospective randomised trial, to treatment with either an uncemented Austin Moore hemiarthroplasty or reduction and fixation with three cancellous screws. Pathological fractures, Paget’s disease and rheumatoid arthritis patients were excluded. Analysis of pre-operative characteristics of patients showed there was no significant difference between the two groups. Mean follow-up of surviving patients was 827 days.
Internal fixation resulted in a reduced mean operative time (22 versus 47 minutes), operative blood loss (23ml versus 171mls) and transfusion requirements. There was no significant differences in the incidence of post-operative complications between treatment other than and increased risk of wound sepsis for arthroplasty (4/207 versus 0/206 deep wound infections). There was a consistent tendency to a marginally lower mortality following internal fixation (15.5% versus 12.7% at 90 days).
Six patients in the arthroplasty group required revision, four for loosening, one for sepsis and one for fracture around the implant. Non-union occurred in 64(31%) of those treated by internal fixation. Most of these patients had conversion to arthroplasty. Other complications of internal fixation requiring secondary operations were avascular necrosis (4 cases), fracture below implant (1 cases) and removal for painful screw heads (7 cases). Functional assessment of the survivors at one year from injury showed no significant difference between the two groups for pain or change in mobility.
These results indicate that arthroplasty for displaced intracapsular fractures in the elderly is associated with a reduced re-operation rate but at the expense of a marginally increased mortality.
A prospective study of 142 consecutive patients admitted with fracture of the neck of femur was performed. 42 patients were operated within 24 hours of time of fracture (group 1), 46 within 24 to 48 hours (group 2) and 47 more than 48 hours later (group 3). Three patients were treated conservatively and in four patients the exact time of fracture was not known.
The reason for delay of the operation was lack of theatre space in the majority of cases (64 patients). Medical problems accounted for delay in only 10 patients.Seven patients out of 42 in group 1 died within four month (16.7%), compared to 11 of 46 in group 2 (23.9%), and 6 out of 47 in group 3 (12.8%). This difference was not statistically significant.
There was no significant difference in requirement for pre- and postoperative blood transfusion between the three groups. No patient operated within 24 hours developed pressure sores. Three patients in group 2, and six patients in group 3 developed pressure sores. Chest infections occurred in three patients in group 2, and in three patients in group 3. None of the patients operated on within 24 hours developed a chest infection, wound infection or urinary tract infection. Two patients who had a Girdlestone procedure for deep infection were operated more than 48 hours after the fracture. One patient requiring drainage for wound infection had the operation 47 hours after the fracture.There were no superficial or deep wound infections, pressure sores, or chest infections if operated on within 24 hours of fracture. There was no difference in the requirement for blood transfusion. Patients operated within 24 to 48 hours of fracture had the highest mortality, although this was not statistically significant.
The perineal traction post has been reported to cause pressure sores, skin necrosis, and pudendal nerve palsy. Tissue pressures of 70 mm Hg applied for two hours have been shown to result in microscopic tissue change whilst pressures of 1.4 kg/cm2 for 90 minutes produced severe or complete nerve conduction block.
To demonstrate perineal traction post interface pressures. To assess effect of padding type on these pressures.
Healthy volunteers were positioned supine on the traction table with the right lower limb supported in flexion and abduction. Longitudinal traction of 40kg was applied to the left lower limb through the boot. Pressures were measured using a pressure pad consisting of individual calibrated inch square pressure cells. The pad was placed around the traction post. Five different types of padding were used on a standard traction post. These were: gamgee, small gel pad, 10cm gel bolster, 10cm soft foam roll and 10cm hard foam roll. With each device, the leg was positioned in neutral, internal rotation, external rotation and adduction. Pressure readings and pain scores were recorded with each manoeuvre.
Maximum pressures were experienced with the gamgee wrap. All subjects noted their highest pain score here. Peak pressures of 100 mm Hg were demonstrated over the ischial tuberosity and adductor tendons. The larger padding devices resulted in significantly lower pressures. Of the different positions, adduction was that which resulted in highest pressures and pain scores, though this was not significant.
The highest pressures exceeded the 70 mm Hg limit known to cause tissue damage. These pressures can be reduced with alteration of the padding. In all procedures it is important to pad the post carefully and use adducted positions for as short a time as possible.
In 1991 15% of the UK population that travelled abroad required medical assistance. We have been treating more patients with lower limb injuries requiring repatriation via aircraft. Recommendations from Airlines were unavailable. 357 Consultants replied to a questionnaire about transportation of patients with a lower limb injury wearing a plaster cast. There was no consensus on safe transportation of these patients. No scientific data is available on the dynamics of transportation of patients with lower limb trauma. In order to assess the safest method of transportation an experiment was conducted. Ethical committee approval was granted. Five volunteers wearing above leg plaster casts were placed in a decompression chamber. The effects on anterior compartment pressures, Doppler venous return, ambient pressure between plaster and skin were assessed in different positions with and without plasters being split. In the normal population we have shown a trebling of intracompartmental pressures from an average of under 10mmHg to 30mmHg. Intracompartmental pressures are more raised with 90 degrees of hip flexion rather than 45 degrees. We recommend patients be transferred with their legs at 45 degrees to the ground with a split plaster cast.
Following fixation of proximal femoral fractures in the elderly the operating surgeon may request that the patient be mobilised partially weight bearing on the injured limb. This instruction is most likely if the bone quality is very poor or the fracture pattern unstable, despite evidence that full weight bearing does not affect outcome.
98 elderly patients with proximal femoral fractures treated by either hip screw device, cannulated screws or hemiarthroplasty, who were previously independently mobile, have been followed prospectively to determine their ability to comply with partial weight bearing instructions.
A specially designed capacitance foot pressure device was used to determine percentage body weight transferred through the injured limb on mobilising under physiotherapy instruction over 5 days, and factors thought to be predictive of success in partially weight bearing were measured using simple ward tests.
14 patients failed to mobilise independently prior to discharge from hospital and were excluded from further analysis. Of the remaining 84 patients only 24 (28%) successfully managed to partially weight bear 30-50% of their body weight on the injured limb. Only six of those who were unable to partially weight bear on starting to walk after surgery had learnt to do so by the fifth day. Factors indicating success or failure were mental test score, grip strength and straight leg raise on the unaffected side.
This study has shown that the majority of elderly hip fracture patients are unable to partially weight bear but, if required, success can be predicted by a few simple ward tests.
It is hoped that this information will lead to the more appropriate use of inpatient physiotherapy resources.
The principle of the sliding hip screw is to provide a controlled collapse at the fracture site. It is during the screw insertion that clockwise rotational torque is imparted to the head and neck
In right-sided fractures the screw causes the head fragment to rotate clockwise leading to apposition or flexed position of the fracture site. In Left sided fractures the clockwise rotation leads to the head and neck fragment into extension of the fracture site leading to a potentially unstable construct.
All intertrochanteric fractures treated over a 12-month period were assessed. 75 fractures were included in the study. The fractures were classified according to Tronzo’s classification (Grades I & II – stable; Grades III & IV – unstable). Intraoperative and postoperative films were assessed for rotational abnormalities in the form of an anterior spike of the proximal fragment in left-sided fractures and a flexed position of reduction in right-sided fractures.
There were 39 Left sided fractures and 36 Right sided fractures.
A rotational abnormality was seen in 11 Left sided fractures compared with none on the right side. All 11 abnormalities were seen in Grade III and IV fractures (2 and 9 respectively). Analysis of results using the Chi-Square test revealed a significant difference (p < 0.001). 3 out the 11 fractures with rotational anterior spike had an implant cut out which needed revision surgery.
Compared to stable fractures, the accuracy of reduction determines the final stability in unstable fractures. In these fractures the rotational torque imparted to the proximal head and neck fragment can cause loss of reduction leading to potential failures of fixation. This appears to be greater in left sided fractures where the rotational torque causes the anterior spike which when not butressed inferiorly and medially can lead to a state where the implant cannot control the shear forces at the fracture site. This can then lead to failure of fixation.
In right-sided fractures the rotational torque often causes compression of the head and neck fragment into the distal fragment with the creation of an infero- medial butress.
The methods of overcoming this problem are with modifications in the technique. Untwisting the last few threads of the screw after insertion could reduce the anterior spike. The application of digital pressure along the anterior neck or the application of a reduction clamp at screw insertion provides counter rotation.
The results of this study confirm that the problem of torque at the fracture site is not of considerable importance in stable fractures but is significantly so in unstable left sided fractures. This results in a greater predisposition for potential failure of fixation
A randomised, prospective trial comparing the percutaneous compression plate (PCCP) and the classic hip screw was performed for intertrochanteric fractures of the femur in 108 patients. The PCCP offers the ability to stabilise fractures with a minimal exposure and periosteal stripping thus preserving soft tissue cover.
Over a 19-month period all patients with extra-capsular fractures apart from subtrochanteric and pathologic fractures were included. They were classified as per Evans classification.
The patient’s pre-operative haemoglobin, premorbid mobility, medical and mental status were noted. The duration of the procedure, screening time, blood loss and any technical difficulty encountered along with the post-operative haemoglobin, drainage and transfusion requirements, as well as the length of stay in the orthopaedic unit and total length of stay in the hospital were recorded. Results were analysed using the Chi-square test and Student’s test.
The operating time was significantly longer in the PCCP group (mean 59vs49mins,P< 0.05). There was no significant difference between the two groups with regard to the other parameters measured.
There was no difference in the failure rate (2 cut-outs in the CHS group and one screw back-out in the PCCP.) With the device being of fixed single angled design it proved to be unsuitable for 3 patients.
The PCCP would appear to be as good as the more conventional device though it does not confer the perceived advantages of decreased duration of stay or significant reduction in transfusion requirement which are associated with other percutaneous procedures. The device is a single fixed angle one and is therefore not universally applicable to all patients.
To assess the outcome of bicondylar tibial fractures, treated prospectively with fine wire fixation in the Limb Reconstruction Service.
Twenty patients with mean age 56 years with bicondylar tibial plateau fractures, were treated at the author’s institution with fine wire fixation over a three-year period. Ten followed road traffic accidents and four followed high-energy falls; The remainder mainly in the elderly resulted from a simple fall. There were four Schatzeker type V, and sixteen type VI. Four were open fractures (Gustilo grade III); Seven patients sustained associated fractures at the same time. They were treated according to a prospective protocol and were followed up for an average of thirty months, (11 – 51). The protocol included CT Scan Guided planning, closed reduction if possible and percutaneous interfragmentary screw fixation to reconstruct the articular surface, under image intensifier control; The external fixator was applied in neutralization. Mobilization and full weight bearing was encouraged as early as possible
Ten patients started full weight bearing between four and six weeks post operatively, in nine cases with other injuries weight bearing was delayed. All patients healed with an average time in the fixator of eighteen weeks, (9–25).
Fifteen patients had a range of movement from Zero to at least 120 degrees flexion. Using Rasmussen’s functional and radiological scoring system, fifteen out of twenty scored good or excellent. Complications included deep vein thrombosis in one patient, loss of fracture reduction in three, superficial pin tract infection which resolved with local pin care and a short courses of antibiotic in five patients, there was no deep infection.
The Sheffield hybrid external fixator is strong, permits early fracture recovery and weight bearing and may have significantly contributed to the high rate of good results in this group, of which more than 50% were over sixty years old. This technique is recommended for treatment of this difficult fracture.
In tibial plateau fracture, anatomical reduction of articular surface with stable fixation can restore the mechanical axis and allow early mobilization. Concomitant management of ligamentous and meniscal injury is essential for preservation of knee function. Open reduction and internal fixation has a significant complication rate.Percutaneous,fluoroscopically and arthroscopically assisted osteosynthesis with special fracture reduction and fixation technique can achieve the purpose of management of tibial plateau fracture, while limiting the soft tissue damage.
18 cases, including all J. Schatzker’s type of tibial plateau fracture, were operated with minimal access surgical technique. Male patients were predominant. The age ranged from 22 to 61 (mean 33.5). Detail pre-operatives planning with CT scan were performed in 16 patients. Fluoroscopy, arthroscopy and special fracture reduction and fixation technique were applied to all cases. All 18 cases could be reviewed. Follow up period ranged from 1 to 4 years (mean 2.3 yr.). Outcome was assessed by HSS Knee Score, standing radiograph and arthroscopy (2 cases).
According to HSS score, 14 patients were rated as excellent (100 to 85), 3 good (84 to 70), 1 fair (69 to 60) and none poor (< 60). Subjectively, 14 patients were satisfied with the treatment. 13 patients were working and participating in sport before injury. 15 took no analgesic, 2 took it once a week and 1 more often. In standing radiograph, only 2 patients showed minimal narrowing of joint space. There was no significant complication directly associated with the procedure.
Percutaneous, fluoroscopically and arthroscopically assisted osteosynthesis is a safe and effective minimal access surgical procedure. Precise pre-operative planning and special fracture reduction and fixation technique are all crucial for success. Short-term clinical outcome is encouraging.
A carbonated apatite cement with a high compressive strength was used in the treatment of tibial plateau fractures. There were 41 patients (20 male; 21 female; mean age 59 years). All patients had isolated tibial plateau fractures.
There were 15 B2.2, 23 B3.1 and 3 B2.3 fractures. Fractures were fixed with limited internal fixation using a short anterior parapatellar incision. Reduction and fixation were initially achieved. Once this was carried out the void under the elevated plateau was filled using calcium phosphate cement. A buttress plate was used in one case, screws or K-wires in 33 cases and calcium phosphate cement alone in 7 cases. Patients were mobilised partially weight bearing in a hinged knee brace and allowed full weight bearing at 6 weeks.
Reductions were anatomic (< 2mm displacement in 32 (78%) cases, satisfactory (3-5mm displacement) in 7 (17%) cases and imperfect (> 5mm) in 2 (5%) patients. Extrusion of some calcium phosphate cement into surrounding soft tissue occurred in one case. This material resorbed with no adverse effects. Loss of reduction was observed in 6 (15%) cases. There were no other significant complications. Thirty-seven patients (90%) had more than 120 degrees of knee flexion at 6 months.
Calcium phosphate cement is an alternative to the use of bone grafting in any area of cancellous subject to compressive load. It is ideal for use in tibial plateau fractures with compressed subchondral bone after elevation. It obviates the need for buttress plating and bone grafting and there is no bone graft donor site morbidity. Patients are able to mobilise more rapidly and early discharge is facilitated.
Calcium phosphate cement is a promising development in the management of tibial plateau fractures and initial results suggest it may be more effective in maintaining reduction that standard methods of fixation and grafting.
31 cases of high-energy proximal tibial fractures were retrospectively analysed. The series included 22 cases of Schatzker VI and 9 cases of proximal tibial extraarticular fractures. There were 7 females and 24 males, with average age being 45years(26–94). There were 12 open fractures ( 1 Gustilo grade1, 10 grade 3b and one 3c); while 19 cases had Tcherne’s grade 2–3 injury. 4 patients developed compartment syndromes requiring fasciotomy. All fractures were treated with preliminary ligamentotaxis using a unilateral external fixator. In addition, Open fractures underwent radical debridement with the one case of 3c requiring vascular reconstruction. CT scan was then done to assess the joint incongruity ,anatomy of the fracture, and to aid in decision making. The fractures were then fixed using percutaneous techniques and a circular external fixator. Minimal open reduction was resorted to in cases with significant joint depression. In all, 26 cases were managed using percutaneous techniques alone while 5 required minimal open reduction and screw fixation. Bone grafting was done in 6 cases and 11 required a plastics procedure for soft tissue reconstruction. The results were assessed using the radiological Rasmussen’s criteria and the clinically using he IKSS knee score. At a mean follow-up of 31mths, the mean time to metaphyseal union was 18weeks (6–25weeks);. 28 patients had good to excellent clinical scores, while 3 had a fair result. The radiologic assessment graded 12 cases as excellent and 19 as good. Complications included 2 cases with flap edge necrosis, 2 with severe pin tract sepsis, 1 with proximal DVT and one case with septic arthritis.
We conclude that the above treatment protocol yields promising results, preserving good knee function without prejudicing future need for arthroplasty.
This study assessed the role of Ilizarov technique, using soft tissue distraction, in correction of radial club hand deformities.
Five patients (6 deformities) with grade IV radial hemimelia (radial aplasia) were studied. There were three boys and two girls aged 2 to 8 years. One boy had bilateral involvement with TAR syndrome. One girl had bilateral involvement with VATER syndrome. One other boy had unilateral involvement with Holt Oram syndrome. The thumb was absent in three cases and hypoplastic in one case. The preoperative deformity measured 95 degrees (range 60–105 degrees). This was corrected using gradual soft tissue distraction with an Ilizarov fixator. Complete correction of the hand deformity was achieved over a period of 4–6 weeks. In two hands, rebalancing tendon transfers were performed in order to try and maintain correction. Following frame removal in both these patients, the deformity recurred despite splintage. Subsequently, four hands were treated with tendon transfers along with wrist stabilisation using intramedullary K-wires. The correction was maintained in all these cases.
It is concluded that the Ilizarov technique can be used to achieve complete correction of radial club hand deformity but that correction can only be maintained by intramedullary stabilisation. The technique is well tolerated by patients and is more physiological when compared to the conventional treatment with wrist centralisation.
Vascularized bone grafts (VFG) have brought great benefits in the field of reconstruction of the lower extremity. However, complications such as fracture of the grafted fibula and delayed union are sometimes seen. Not only to prevent these complications but also for stability after fracture of the grafted fibula, the Ilizarov external fixator is a very useful option. We report here the clinical results of cases treated by VFG combined with Ilizarov external fixator for reconstruction of the lower extremity.
We have performed 53 vascularized fibula transfers to reconstruct lower extremities. An Ilizarov external fixator was used for the initial immobilization in 7 (2 femur, 5 tibia) and for delayed union or fracture of the grafted fibula in 2 cases of congenital pseudoarthrosis of the tibia.
All patients achieved good bone reconstruction. All are able to walk without a brace except for one congenital case. The average period to achieve bony fusion was 13 months in femur cases, 6 months in adult tibia cases and 2 months in congenital cases. The average periods to walk without a brace were 14 months, 8 months and 10 months respectively. However, it took 9 months and 28 months to achieve bony union in the cases with delayed union or fracture of the grafted fibula.
In the reconstruction of the lower extremities using VFG, the determining factor in method selection is whether sufficient mechanical support is available. An Ilizarov external fixator for immobilization permits the patient to walk as soon as possible. Dynamization from this semi-rigid external fixator causes bone hypertrophy and improved incorporation of the graft.
Although total elbow arthroplasty is undertaken in far smaller numbers than total hip and knee arthroplasty a recent review of the world literature indicated that aseptic loosening radiologically occurred in 17.2% whilst clinical loosening was present in 6.4%. In addition, infections were noted in 8.1%
With both aseptic and septic loosening bone loss can be a major problem and must be addressed if revision surgery is contemplated Options for treating bone loss include:
Revision with standard implant Revision with customised implant Revision with impaction bone grafting and standard or customised implant Revision with allograft and standard or customised implant
When considering revision surgery it is essential to ascertain whether or not implant loosening is aseptic or septic. To this end screening blood tests including white blood count, ESR and CRP should be performed. A bone scan may also be helpful. In addition, it is my practice to perform an aspiration biopsy prior to revision surgery. A sample of fluid from the elbow joint is looked at microscopically and cultured for organism sensitivity.
If infection is present surgery is undertaken as a two-stage procedure. The first stage involves removal of the implant and bone cement together with the insertion of antibiotic beads specially prepared with added antibiotics appropriate to the sensitivity of the infectiong organism.
If infection is not present then a one-stage revision is performed.
A prospective study on total knee replacement in patients with Juvenile Idiopathic Arthritis was carried out. There were 31 knee replacements in 17 patients; 12 were female. Bilateral procedures were performed in 11 patients; 10 staged during a single admission and 1 performed in a single procedure. The mean age was 19 years (range, 14–26), and the mean follow-up was 23 months (range, 6–44). The surgery was complicated in 9 cases by a previous distal femoral osteotomy. The results were assessed using the Hospital for Special Surgery (HSS) scoring system. A cruciate sacrificing implant was used in all cases, and the patella was resurfaced in 25/31.
The pre-operative mean arc of motion was 62° (range 10°–90° ) and this averaged 89° (range, 20° –115°) at latest follow-up. The pre-operative mean fixed flexion 17° (range, 0° –15° ). The mean pre-operative HSS score was 36 (range, 8–59), and the mean at latest follow-up was 81 (range, 67–95). There has been no sign of aseptic loosening on serial radiographs over the follow-up period. One patient developed a deep infection at 20 months requiring a 2-stage revision and one patient developed a perforated duodenal ulcer postoperatively.
The clinical results are very satisfactory, allowing patients to regain their mobility and independence. The early radiographic results are very encouraging despite the poor bone quality and severe deformities that require correction.
The history of the development of the Kudo elbow replacement was illustrated from the original Type 1 prosthesis in 1971 to the current Type 5 manufactured in cobalt-chrone and high-density polyethylene from 1994. The results of the Kudo Trial were presented. In this prospective trial all patients had rheumatoid arthritis with at least grade 4 or grade 5 changes on the radiographs. The procedure was carried out by the same surgeon in every case using a posterior approach. The patients were reviewed at regular intervals and the results presented are of those patients at their five-year follow-up.
There were 105 joints replaced in 84 patients (61 females) with an average age of 63 years. Five were revisions of previous implants. Relief of pain was very significant in all cases with only 8 patients experiencing “mild” symptons. The total gain in range of movement was 33° with 10° improvement of extension and 23° of flexion.
The complication rate was low with only one patient having pronounced ulnar nerve dysaesthesia although four had a mild persistence of sensory symptoms.
There were six cases of infection. Three of these were superficial with negative cultures. Three had positive cultures, all staphylococcus aureus and one of these was revised, following gentamicin beads, to a custom built prosthesis and remains clinically and radiologically satisfactory nine years later.
One ulnar component became loose at five years and was satisfactorily replaced with a long stemmed pros-thesis. Radiological “lucent lines” are variably seen and their long-term significance is not fully known.
A survival analysis was carried out using the method of Murray et al, which gave a 10-year survival of 86.7%.
Pin clamp motion was continuously monitored using a displacement sensor as patients walked with a dynamic fixator applied. Patients with a shaft fracture, nonunion or lengthening of the tibia were monitored, all of whom were in the stage of dynamization. The Hifixator equipped with a ball bearing mechanism on the inner surface of its dynamic pin clamp was used as a dynamic external fixator. The aim of this study was to estimate the magnitude of movement and the type of deformation occurring at the fracture site or callus generated after distraction osteogenesis. The actual motion of the bone fragment has components with six degrees of freedom, which are transferred to the pin clamp. The magnitude of the displacement of the pin clamp along the shaft is expressed by an equation involving these six components. If the pin clamp has a sufficiently smooth sliding surface and a small clearance between it and the shaft, and the pin clusters are sufficiently rigid during walking, the amount of the displacement can be expressed by the linear combination of these components.
Accuracy of the measurement was evaluated using a bone model fixed with a Hifixator mounted with a displacement sensor, by performing dynamic loading tests with axial, bending and torsional forces The measured values agreed well with the theoretical values when the rigidity of the bone model was high. The displacement was recorded versus time during more than twenty cycles of walking with weight bearing of the patients. The rhythm of walking was controlled with a metronome set at 0.5 Hz. The displacement curve had an oscillatory component synchronized with a heel strike and a toe off, a time dependent component expressed by shifting of the baseline, and an irreversible component during a non-weight bearing period after walking. The three components were analyzed with a simple Voigt model.
In all patients, both the amplitude of the oscillatory component and the time dependent component expressed as retardation time decreased as healing proceeded, and by the time of fixator removal the irreversible component had disappeared. This method was useful for quantitatively evaluation the viscoelastoplascity of the healing site.
The validation of a new classification of the external fixator screw-bone interface.
Screw loosening significantly affects the stability of an external fixator, however radiographs are normally taken to assess bone healing and not screw loosening. This study was performed to assess the inter and intra-observer reliability of radiographic features of external fixator screw loosening. Eight observers were shown plain radiographs of 120 external fixator bone-screw interfaces on two occasions, and were asked to grade the screws according to the following features.
Solid screw. Periosteal reaction around the screw. Area of lucency around the screw. Marginal corticalisation around the screw. Frank loss of position of the screw.
The overall kappa value for this study was 0.29, with the component values ranging from 0.15 to 0.41. To determine if the reliability could be improved, two observers classified 192 digitised radiographs of external fixator screws. On the first occasion the radiographs were shown at a size, brightness and contrast equal to the original film. On the second occasion the radiographs were subjected to image enhancement and magnification. This showed improvement in all the kappa values, the overall value increasing to 0.39, with similar improvements in the component parts. Unfortunately no observations were made of loose screws, therefore, two observers were asked to classify 160 digitised images of screws which were selected with a bias in their outcome, to remain solid or become loose. The observers obtained a kappa value > 0.50 for loose screws.
A classification system for the bone-screw interface is of value both in research and clinical practice. Despite the fact that standard radiographic views were used the classification system described shows satisfactory inter and intra-observer reliability and this improved when digital enhancement was applied.
To review healing rates, complications, alignment, length and function in non-unions treated with Mono-lateral External Fixation.
A cohort of 110 patients (113 segments) treated for non-union, by mono-lateral external fixation in Sheffield between 1987 and 1996 is reviewed. There were 83 males and 27 females with a mean age of 37.2 years. 67 patients had high-energy injuries and there were 56 open fractures. There were 60 tibiae, 38 femora and the rest were upper limb long bones with a mean of 3.2 previous procedures. The mean duration of non-union was 23.4 months (range 3–123). There were 64 monofocal procedures with 41 supported in neutralisation, 20 in compression and three in distraction. There were 49 bifocal procedures (33 compression distraction and 16 bone transport). 71 segments required a bone graft.
The success rate using the initial fixator was 90%. Clinical and radiological union was achieved in 109 segments (96.5%) although seven required further fixation and one subsequently went on to amputation for ischamia. All five amputations were in smokers and three were directly related to vascular failure.
The mean hospital stay was 21.12 days and the mean number of operations per patients was 2.55.The mean time to bony union was 12.69 months (range 2.5-64). The Length gained mean 4.5 cm (range 1.5-12 cm). Angular correction achieved 12° (range 2-39°); The bony and functional results were assessed at the end of treatment by system described by Paley & Catagni (JBJS 77A, 1995).
Excellent
42%
Good
50%
Fair
0.3%
Poor
0.0%
Amputations
4.4%
Excellent
59 cases
Good
34 cases
Fair
03 cases
Poor
00
Monolateral external fixation can provide stable fixation for the treatment of established non-unions. The fracture environment may be carefully controlled and angulation and length corrected simultaneously. Interestingly 11 out of 12 problem cases were in smokers.
We treated the severe orthopaedic problems,for example, the deformity, the long bone defect and the severe soft tissue contracture,treated by Ilizarov external fixator for ten years. Ilizarov external fixator was used to stabilize the bone fragments and elongate the bone and soft tissue. The purpose of this study is to examine the usefulness and the problem of Ilizarov external fixator.
Materials were 52 patients treated by Ilizarov external fixator.Age was from13 years old to 81 years old. The averaged age was 41.3 years old. The averaged follow up periods was 4 years 5 months.The causes of these diseases were trauma, infection and congenital anomaly etc. We examined the clinical results and the complications of this method.All deformities could be corrected without one patient.The callotasis of these cases were succeeded without one patient.The bone union could be get without one patient.These 2 patients were amputated because of the bleeding due to Idiopathic Thrombocytopenic Purpura and the non-healing of infection. The complications of these methods were fracture (4 cases), infection (2 cases), recurrent deformity (1 case), deformity of the talus (2 cases) and abnormal caltification (2 cases). We could get good clinical results but had some complications.
Conclusion was that Ilizarov external fixator was useful for the treatment of the various kinds of the complicated orthopeadic problems and there were some complications as we used Ilizarov external fixator for the elongation of the soft tissue and bone.
31 cases of high-energy proximal tibial fractures were retrospectively analysed. The series included 22 cases of Schatzker VI and 9 cases of proximal tibial extraarticular fractures There were 7 females and 24 males, with average age being 45 years (26–94). There were 12 open fractures (1 Gustilo grade1, 10 grade 3b and one 3c); while 19 cases had Tcherne’s grade 2–3 injury. 4 patients developed compartment syndromes requiring fasciotomy. All fractures were treated with preliminary ligamentotaxis using a unilateral external fixator. In addition, open fractures underwent radical debridement with the one case of 3c requiring vascular reconstruction. CT scan was then done to assess the joint incongruity, anatomy of the fracture, and to aid in decision making. The fractures were then fixed using percutaneous technique and a circular external fixator. Minimal open reduction was resorted to in cases with significant joint depression. In all, 26 cases were managed using percutaneous techniques alone while 5 require minimal open reduction and screw fixation. Bone grafting was done in 6 cases and 11 required a plastics procedure for soft tissue reconstruction. The results were assessed using the radiological Rasmussen’s criteria and the clinically using the IKSS knee score. At a mean follow-up of 31mths, the mean time to metaphyseal union was 18 weeks (6–25 weeks); 28 patients had good to excellent clinical scores, while 3 had a fair result. The radiologic assessment graded 12 cases as excellent and 19 as good. Complications included 2 cases with flap edge necrosis, 2 with severe pin tract sepsis, 1 with proximal DVT and one case with septic arthritis.
We conclude that the above treatment protocol yields promising results, preserving good knee function without prejudicing future need for arthroplasty.
The purpose of this study is to elucidate the possibility of an ideal joint alignment after monofocal lengthening of tibia in achondroplastic patients. In 10 cases of the alignments of knee and ankle joints of tibias in which plane radiographs were examined.Unilateral fixators were applied to both tibias,after lengthening in the normal manner, deformity was corrected manually in a single procedure without anesthesia. In order to determine the amount of angle to be corrected, a line was first drawn on the radiograph from the center of the knee joint to the center of the ankle joint. (This line is named the Knee-ankle line: KAL).
Next we drew a line along the ankle joint and measured the angle between this line and KAL. We also drew a line across the tibial plateau and measured the medial angle between this line and KAL. We tried to align the ankle joint perpendicular to KAL and the medial angle between the tibial plateau and KAL at 87 degrees , instead of trying to align the axis of the tibial shaft perfectly straight. The medial angles between the line across the tibial plateau and KAL were corrected to 86 degrees in average, with a range from 84 to 90 degrees, and the medial angles between the line across the ankle joints were corrected to 87 degrees in average, ranging from 80 to 90 degrees in result.
In conclusion, joint alignments of tibias in achondro-plastic patients were able to be corrected successfully without any complications using our monofocal lengthening technique. And severe varus deformities of tibias can be corrected even with monofocal lengthening technique by trying to correct the alignments of knee and ankle joints rather than trying to straighten tibial shafts.
To determine whether reducing the splintage rate in DDH patients had any effect on the rate of surgical procedures for the treatment of DDH. .
Since 1991, in the Blackburn region, there has been a limited target ultrasound screening programme for developmental dysplasia of the hip.
The detailed records of the demographics, clinical and ultrasound findings, treatment and outcomes of all children screened by the senior author were reviewed.
In 1996 and 1997 only those with persistent major dysplasia at 8 weeks and those with dislocatable hips were placed into Pavlik harnesses.
In 1998 only those babies with persistent major dysplasia at 8 weeks of age, or persistent hip instability at 1–2 weeks were placed into Pavlik harnesses.
The splintage rates, late dislocation rates (diagnosed after 6 mnths of age) and surgery rates were determined.
During the study period 11164 babies were born in the region. 797 (7.1%) babies were seen by the senior author.
Surgery in early irreducible hips is unavoidable. Surgery in late dislocators is only avoidable by changing from a selective ultrasound screening policy to performing ultrasound screening on every baby born.
With a limited hip screening programme and clinical and ultrasound monitoring of patients, splintage rates can be minimised without increasing the rate of surgery for developmental dysplasia.
No child who would have been splinted by the criteria used by other centres, and who wasn’t splinted in this series, required surgery.
A prospective evaluation comparing functional results in conventional and percutaneous femoral nailing techniques was performed.
4 patients (8 nails) were operated on with a conventional IM nailing technique (CT), and 4 (8 nails) with the percutaneous technique (PT).
Limited trochanteric approach was performed, allowing the setting up of the sighting device for the nail.
Patient was positioned on the lateral side, hip at 60° flexion. A long k-wire was passed through the skin, along the axis of the medullary canal in the anterior-lateral part of the Piriformis fossa, into the medullary canal. A small skin incision was performed, and then a cannulated drill introduced over the k wire. The reamer guide was pushed down to the distal femoral metaphysis. Percutaneous flexible reaming was then performed in a conventional manner, taking care to introduce the reamer through the gluteus medius with no torque. Section was performed through the same incision with a modified intramedullary saw. The nail was inserted, fixed on a modified sighting device. The continuous passive machine was set up in the recovery room or in the intensive care unit. Physiotherapy was directed towards maintaining knee range of motion. Patients were evaluated for scar size, muscle function, leg raise and range of motion (ROM).
Follow-up averaged 30 (CT) and 11 (PT) months. Gain averaged 61 mm (CT) and 79 mm (PT). Scar size for nail insertion ranged from 6 to 11 cm (CT) and 1.1 to 3 cm (PT). Total number of operations from nail insertion to removal, including GA for ratcheting (GAR) and GA for other complications (GAC) was: 18 (CT, all nails removed) 9 (PT, among them 3 removal operations on the waiting list). On postoperative day 1, all patients with PT returned to a subnormal ROM. At one week, Knee flexion averaged 93° (CT) and 131° (PT). For CT, it increased gradually, passing 100° at 8 weeks, and 130° at 20 weeks. In PT, the minimum obtained was 126° at 10 weeks, passing 130° at 13 weeks. In CT, the decreased knee flexion was 90° (5 knees) and 80° (1 knee), while in PT; only 2 knees went below 110° (85 and 95°). Trendelenburg sign was negative in all PT by 3 months.
Percutaneous IM nailing, along with a good physiotherapy programme, seems to improve tremendously the outcome and decrease the complication rate, even in large limb lengthenings, which are considered as major surgery and often are associated with numerous complications.
In this study we highlight the advantages supported by long term results of using our external fixator system for femoral derotation osteotomy as part of our management regime for developmental dysplasia of the hip. Out of all the children in the East Kent area who present with a dislocated hip each year about 4 require a femoral derotation osteotomy in order to maintain a good position after either open or closed reduction.
The system has been used since 1981. 51 patients (56 hips) were reviewed with a follow up between 5 and 18 years with a mean of 11 years. The age at diagnosis ranged from shortly after birth to 42 months with a mean of 12 months. The treatment involved a protocol in which traction was applied for 4 weeks preoperatively if the hip was high and open or closed reduction was selected according to the result of an arthrogram. 33 of the 51 patients received traction and 23 patients (25 hips) had an open reduction. Following reduction the hips were immobilized in a spica for 6 weeks after which the femoral osteotomy using the fixator was performed. A second 6 week period of spica immobilization followed after which the fixator and spica were removed. We had 16 complications including 3 patients who developed AVN of the femoral head. 8 patients required an additional 16 operations.
We assessed the patients clinically and radiologically using the Severin’s grading system. At final follow up over 85% of patients were assessed to have a clinical grade of 1 and 2 and over 70% a radiological grade of 1 and 2.
Our technique of external fixation has several advantages over conventional methods of fixation of the femur: a) the avoidance of a 2nd open procedure to remove the implant, b) the accuracy of the femoral derotation using the goniometer and c) the achievement of femoral fixation without the need for image intensifier screening.
As the number of patients being offered multifocal procedures in limb reconstruction surgery has increased a study was performed to compare single stage and staged procedures.
A retrospective analysis of all multifocal procedures (more than two sites) performed between 1988 and 1997 was carried out looking at treatment times, results and complication rates. A total of 51 multifocal procedures were performed. The mean number of sites operated on was 3.8 per patient for single stage and 4 per patient for staged. There were 18 single stage and 33 staged operations. There were 29 performed on the paediatric age group for indications such as achondroplasia and short stature. The rest were in adults where the main indications were related to complex trauma management and their complications. External Fixation was the principle method of treatment.
The total hospital stay averaged 18 days for single stage procedures and 29 days for staged. Of the single stage cases 12 had one operation with a mean of 1.33 operations (including surgery for complications) compared to staged procedures which had an average of 2.8 operations (range 2–5 ). In addition, the total treatment time (time of first surgery to discharge) was more for staged surgery, 5 years compared to 3.6 years. In the single stage group 9 patients (50%) had at least one significant post operative complication (2 severe, 7 moderate) and in the staged group 19 (57%) had significant complications (3 severe, 16 moderate). There was no detectable difference in the final clinical result obtained between the groups.
From this study we would conclude that single stage procedures carry no increased risk and are of benefit to patients because of the shorter hospitalisation, reduction in the number of operations and general anaesthetics and the reduced time to final outcome.
To assess the outcome of Quadricepsplasty in limb reconstruction for stiff knees, and to analyze the contributing factors.
Thirteen patients underwent quadricepsplasty over the last 11-years for severe extension contractures of the knee, in the Limb Reconstruction Service. Ten cases were posttraumatic treated with External fixation, and three were non-traumatic causes, with an average interval between injury and quadricepsplasty of 10 years (range, 2–55). Eight patients had leg lengthening with an average of 6.5cm (range, 3–14), with simultaneous deformity correction. Post-operatively all the patients had continued passive motion except one with a fused hip.
Two to six weeks post-operatively, nine patients necessitated manipulation under anesthesia due to noteable loss of movement.
Preoperatively the average flexion was 24°(10–40), which improved in the operating room to 98°. After an average follow up of 15 months post-operatively they lost a mean of 18° flexion, with a final flexion 80°. Three patients developed an extension lag of 10° post-operatively. Two had deep infection with unsatisfactory results. Using Judet’s classification, we had 8 (53%) excellent or good, 6 (40%) fair, and one poor (7%) result.
The unsatisfactory results were associated with deep infection, long fixator time and a long interval between injury and quadricepsplasty.
Quadricepsplasty provides good results for severe extension contraction of the knee. Judet’s technique of disinsertion and muscle sliding addresses the problem of pin site tethering on the lateral side of the femur. Since this procedure is not free of complications and always demands intensive postoperative rehabilitation, it should be reserved for patients with severe extension contraction.
Congenital dislocation of the patella requires early surgical reduction for better walking. We studied the results of our combined soft tissue procedures performed on 6 knees in 5 children. The age at surgery ranged from 3 to 12 years with a mean of 5.3 years. The follow-up period ranged from 3 to 9 years with a mean of 5.1 years. Underlying diagnoses were fibular hemimelia in one knee, congenital dislocation of the knee which was reduced without surgery in two, and nail-patella syndrome in three.
The surgical procedures involve lateral release to reduce the patella, resection and tightening of medial capsule and semitendinosus transfer to the patella. Quadriceps lengthening was also required in two knees. After lateral release, the semitendinosus tendon is detached at its insertion, and is pulled out at the musculotendinous junction. Then, the tendon is pulled down to the patella under the skin, and is passed through a drilled tunnel in the patella from superomedially to inferolaterally. Finally, the tendon is reflected and sutured to the anterior surface of the patella under sufficient tension at 20 degrees of knee flexion.
The five knees operated on under 5 years of age were well reduced and well positioned in the femoral groove at follow-up. The one knee operated on at the age of 12 years showed subluxation. Episodes of giving way and abnormal gait disappeared after surgery in all the patients. Femoral groove depth increased after surgery. The improvement in the young infants was better than in older child. We found that the transferred semitendinosus tendon acts well to maintain good patellar position during knee flexion.
We conclude that early surgical reduction is extremely important and it will stimulate proper development of femoral groove, and semitendinosus transfer combined with lateral release is effective to keep the patella in its groove during knee flexion.
To determine whether the spectrum of genetic mutation in Hereditary Multiple Exostoses supports a neoplastic aetiology for this condition.
Historically, experts have been cautious in attributing neoplastic qualities to the osteochondroma. Solomon states ‘[osteochondromas] are not neoplastic in the ordinary sense of the word’; Morton that it ‘is not a tumour but a growth-aberration; Peterson that the ‘osteochondroma is not a true neoplasm’; and Schmale that ‘exostoses are the result of dysplasia of the lateral apect of the growth-plate’. There are, however, several features of osteochondroma behaviour common to other neoplasms which suggest a neoplastic aetiology:
the existence of an autosomal dominant inherited multiple form, in which lesions are histologically identical to the solitary form. lesions which are distributed randomly and perhaps asymmetrically at ‘high-risk’ anatomical sites (usually adjacent to those physes with greatest growth potential). evidence of behavioural or cellular disorder. a potential for malignant transformation.
Recent genetic data has supported a fresh look at the neoplastic nature of osteochondromas. EXT1 and EXT2 genes are responsible for Hereditary Multiple Exostoses (HME). EXT1 codes for a protein which alters the synthesis and display of cell-surface heparan sulphate glycosaminoglycans; molecules which affect cellular growth, differentiation, motility and adhesion. Loss-of-function of such a gene may initiate a neoplastic pathogenesis in osteochondromas.
From 1996–1999, 51 families with HME were screened for EXT mutation, with mutations identified in 41 families. EXT mutation was assessed by means of fluorescent single-strand conformational polymorphism (f-SSCP) screening, followed by sequencing analysis.
All frame-shift, splice-site and nonsense mutations are loss-of-function. Missense mutations may result in partial or complete dysfunction if a crucial folding or binding site is involved. Since no missense mutations were new, this suggested their mutation sites are important, and may effectively result in loss-of-function. These data strongly support a tumour suppressor gene function for EXT genes, and a neoplastic pathogenesis for HME.
The use of antenatal abdominal ultrasound (AAU) in the diagnosis of clubfoot is established. The accuracy of the investigation is unclear, leaving difficulties for the clinician involved in counselling parents.
This study was conducted to investigate the accuracy of AAU in the diagnosis of clubfoot. We assessed the AAU findings of mothers of 20 children with varying degrees of clubfoot deformity between 1993 to 1998. There were 12 males and 8 females; 30 feet were affected - 6 were left, 8 right sided and 8 were bilateral. There were two sets of twins, each with bilateral deformity. The mean foetal age at diagnosis was 23.4 weeks ( range 18–35 weeks).
Three patients had oligohydramnios and two had polyhydramnios. One patient had an amniocentesis that was normal. Karyotyping was not performed. There were no false positive or false negative results.
Our results show 100% concurrence between the scan results and the clinical findings at birth. Three clubfeet were reported as being positional; their clinical diagnoses revealed a mild deformity that needed no treatment other than reassurance and advice. Twenty one feet were treated with physical therapy, manipulation and serial castings. Six feet required surgery.
AAU in the second trimester of pregnancy is a reliable method of diagnosing clubfoot, and the parents can be counselled with confidence regarding management. As AAU is currently offered to almost all pregnant women, it can be expected that more cases of clubfeet will be diagnosed in the antenatal period. An orthopaedic surgeon must be prepared to counsel parents even before a clinical examination is possible.
The Cincinnati incision is widely utilized in clubfoot surgery and allows excellent access to the medial, lateral and posterior structures involved. Closure of the skin at the end of the procedure without undue tension may be difficult. Wound necrosis and excessive scarring may occur and may lead to inadequate correction. One alternative is to splint the foot in an initial equines position post-operatively with repeat cast changes to achieve optimal position once soft tissue swelling has decreased. A further method is to leave the wound open and allow it to granulate.
The healing and final cosmetic appearance of wounds allowed to heal by granulation following the Cincinnati incision were reviewed.
We reviewed 14 feet in 10 patients who had undergone partial closure of the Cincinnati incision following peritalar release. The majority of the children were male and the average age at surgery was 28 weeks. All corrections were performed as primary procedures on patients with idiopathic CTEV. At the end of the procedure an above-knee plaster was applied. The plaster was changed weekly in the outpatients department until the wound had healed. Patients were maintained in plaster for 12 weeks.
All final wounds were cosmetically acceptable both to the surgeon and the parents. The widest scar was 3 mm and the average time to heal four weeks. No infection had occurred although two wounds were treated for overgranulation.
Partial wound closure of the Cincinnati incision avoids undue tissue tension and allows a fully corrected position of the foot to be maintained at the end of the initial procedure. A second anaesthetic to obtain further correction is therefore avoided. Partial wound closure leaves cosmetically acceptable scarring with minimal complications. Parents should be warned about the initial appearance of the wound but may be reassured regarding final outcome.
To assess the results and complications of this method in a consecutive study of 99 segments with a 5 year follow up
The Vilarrubias method of limb lengthening aims to reduce soft tissue tension and protect joints in order to achieve longer lengthenings with fewer complications. Between 1988–1993 we operated on 99 segments using a modification of this method. The procedure combines a Wagner fixator with percutaneous soft tissue releases, static joint splintage and non-weightbearing mobilisation in a semi-reclining wheelchair. During the consolidation phase the fixator is removed and a moulded plaster applied. In Sheffield we used the Orthofix lengthener and permitted weight bearing and dynamisation in the consolidation phase. The criteria for patient selection were a lengthening aim of greater than 20% of the original bone length or other at risk features (Saleh and Hamer). There were 54 children, 19 with short stature and 35 with asymmetry, age range 4–19 years.
The mean length gained was 92 mm (range 21–173) and the mean BHI 41.3 days/cm (range 16.9–308). In 19 patients there were no complications. In the remainder there were 47 pin site problems, 33 flexion contractures, 33 angular deformities and 15 stress fractures. There were no deep infections or neurological sequelae. Some complications such as flexion contracture; angulation of the regenerate and stress fracture could be secondary to excessive soft tissue tension. Therefore, the length gained and BHI was compared for segments with these complications and those without, using the Students t test, and this was not significant (p> 0.15).
The method appears effective in achieving long lengthenings. Callus formation was satisfactory despite long periods non weight bearing. Considering the lengthening aims and high-risk cases it compares favourably with other reported series. We believe it remains an effective technique for cases of intermediate complexity.
We treated patients with severe slipped capital femoral epiphysisor SCFE with a posterior tilt angle or PTA of greater than or equal to 60 degrees with a Sugioka transtrochanteric rotational osteotomy. We report on the clinical and radiologic results of tis method.
The study was performed on 8 cases (including 9 hips) of slipped capital femoral epiphysis, for which transtrochanteric rotational osteotomy of femoral head (Sugioka method) was carried out in author’s department from 1987 to 1996. The age of onset ranged from 9 to 14 years old (average: 11.6 years). There were 4 boys (4 hips) and 4 girls (5 hips). The follow-up period ranged from 2 years to 10 years (average: 4.4 years). Three of the treated hips were classified as chronic and 6 as acute on chronic. Preoperative head-neck angle (HNA) was 64 – 83 degrees (average: 68 degrees). All patients were performed a transtrochanteric rotational osteotomy of the femoral head which is known as the Sugioka method. The rotational angle was from 70 degrees to 90 degrees. The presence of pain, postoperative range of motion, PTA on postoperative X-rays, avascular necrosis and osteoarthritic change were examined as part of the evaluation of the clinical results.
Necrosis of femoral head was found in one case, while no pain was noted in the other cases, and the range of motion was generally satisfactory. In the radiologic results, PTA was improved to 10 – 25 degrees (average: 18.5 degrees).
Necrosis of femoral head was observed in one hip, but the results were satisfactory in 7 cases (8 hips). These results suggest that this technique is useful for the treatment of severe cases of slipped capital femoral epiphysis
Over the last 30 years 215 Chiari medial displacement pelvic osteotomies have been carried out, principally for dysplasia of the hip, presenting after adolescence or following previous surgical treatment. Substantial pain relief was achieved initially in 93 per cent of the patients, particularly when the osteotomy was undertaken before stiffness and arthritic change had developed. Survivor-ship analysis, using revision of the hip as the index of failure, revealed that there was a progressive deterioration of the result with time, but that almost 4 out of every 5 hip joints were functioning acceptably at 25–30 years.
The radiographic characteristics of 110 osteotomies in 89 patients were evaluated 5-30 (mean 18) years after surgery which was performed at the age of 15.9+-9.5 years. Revision was significantly (p < 0.05) more likely in those patients operated upon after the age of 25 years. The centre-edge (CE) angle increased from 2.5+-13.9 degrees preoperatively to 41.8+- 15.0 degrees immediately after operation; the increase in the CE angle was maintained at long-term review (39.5+-16.5 degrees), and even with severe dysplasia (CE angle less than zero) a substantial improvement in femoral head cover was achieved, usually by the medial shift of the lower pelvic fragment. However, the femoral head was not invariably medialised by the osteotomy and lateral movement of the ilium was noted when the preoperative position of the joint was relatively medial, or when the hip was arthritic. In the longer term pelvic remodelling did not reverse the medialisation produced by the osteotomy, and femoral head cover was maintained. The osteotomy is at its most effective between the ages of 10–35 years and is not recommended above the age of 40 years.
Using a lateral approach during which the greater trochanter is excised, we performed domical pelvic osteotomy (modified chiari’s prpcedure) different from the original Chiarifs procedure. In a series of 176 modified Chiari pelvic osteotomies in 175 patients over 40 years old of the advanced coxarthrosis with acetabular dysplasia , in whom the postoperative courses were followed for more than 5 years (average, 6.9 years). JOA hip scores were improved in pain from 15.6 to 34.2 points and a total JOA score was improved from 55.7 to 76.5 points ,almost satisfactory results were obtained in 72.8% . In particular, markedly satisfactory results were obtained with respect to the improvement of pain in 84%. Radiographically, the coverage of the femoral head was markedly improved .The joint space was more dilated in 55% compared to that before surgery., however, the stage of coxarthrosis was more advanced in 18patients . In addition, the pathologic conditions of coxarthrosis had clinically deteriorated in 11 patients, resulting in treatment by total hip arthroplasty. As a result, there were more satisfactory results obtained, even in patients with advanced coxarthrosis, than expected.
Based on the results of this study, we considered that the Modified Chiari’s procedure is most effectively indicated for mature patients with the flat headed hip joints complicated by acetabular sclerosis. Therefore, we perform this procedure in combination with femoral valgus osteotomy. In contrast, satisfactory results cannot be expected from this combination therapy particularly in patients with the atrophic type roundheaded hip joints exhibiting poor acetabular sclerosis.
It is considered that the Modified Chiari’s procedure will be a useful treatment modality substituting for total hip arthroplasty even in mature patients, if applicable cases are carefully selected.
Subsequently, we radiographically evaluated the prognosis of the acetabulum based on its preoperative status. Levels of acetabular sclerosis were classified into the following 3 grades : : atrophic, nornopholic and hypertrophic type.After surgery, the joint space was dilated or maintained in all patients with the hypertrophic type hip joints. However, most patients with the atrophic type hip joints showed the poor prognoses because the stage of coxarthrosis was further advanced in 18% of them. Concerning the capital morphology before surgery, when the prognoses were evaluated based on the preoperative capital morphology, 96% of the proliferative headed hip joints were successfully treated, while only 83% of the round headed hip joints were successfully treated.
Even when the stage of coxarthrosis advanced during the prolonged period of follow-up and total hip arthroplasty is performed, it is the merit of this procedure that a larger size cup be applied without bone grafting.Because the matrix is formed satisfactorily in the newly generated acetabulum where osteotomy was performed.
The present study evaluated the results of the Modified Chiari’s procedure performed mature patients with advanced coxarthrosis caused by acetabular dysplasia . Clinically, the JOA score was markedly improved in 84% patients. Radiographically, the coverage of the femoral head was more delated in 52%, compared to the joint space before surgery. However, the joint space narrowed in 18 patients, and total hip arthroplasty was performed in 6.3%. Modified Chiari method was considered to be a useful treatment modality that can sufficiently substitute for total hip arthroplasty in selected cases.
Anterior knee pain attributable to the patellofemoral joint and extensor mechanism dysplasia is a common presentation to Orthopaedic surgeons. Plain radiology is likely to remain the primary investigation of the knee in most centres, but most of the radiological features of extensor mechanism dysplasia are time consuming and difficult to measure reproducibly. 137 consecutive symptomatic knees aged under 30, referred to an Orthopaedic surgeon were studied in order to identify a rapid and reproducible marker for those knees worthy of further in-depth analysis.
Overall, 67 knees (49%) had at least one radiological abnormality and 70 (51%) were considered ‘normal’. There were 5 Dejour Type3 dysplasias of the femoral trochlea, 9 Type2 and 12 Type1. There were 49 cases of patella alta and 5 of patella infera. Four knees had an abnormal lateral patellofemoral (patellar tilt) angle. 15 knees had more than one abnormality. The classification of trochlear dysplasia was difficult and showed poor reproducibility. This was also true for the measurement of lateral patellofemoral angles. Patellar height was more easily measured but took time. The sulcus angle emerged as an easily and rapidly measurable feature that was reproducible and was closely related to the other features of extensor mechanism dysplasia.
The sulcus angle offers a rapid and reliable ‘screening’ measurement on knee radiographs. A normal sulcus angle suggests that seeking the other radiological markers of extensor mechanism malalignment is unlikely to reveal additional useful information. Other diagnoses can then be sought. The more abnormal the sulcus angle, the more severe the other features of extensor mechanism dysplasia are likely to be. Further detailed measurements can then help to define the most appropriate surgical correction.
This paper looks at the physical findings, microbiology and haematological results of one hundred cases of septic arthritis.
The commonest joints to be involved are the knee (43 patients) and the shoulder (39 patients). The commonest organisms cultured were salmonella typhi (19 patients), salmonella enteritidis (13 patients) and staphylococcus aureus (11 patients). Most patients are anaemic (mean Hb 8.7) and underweight (mean 74% of expected weight for age). Ten patients were found to be HIV positive and two sickle cell positive.
The pathogenesis of septic arthritis in this group is discussed. It is likely that there is a widespread subclinical salmonella bacteraemia in this population as there is a high incidence of diarrhoeal disease. The reason for the high incidence of shoulder infection is not clear. It has been noticed that most children are carried on their backs by their mothers and lifted up for this by their arms. It is therefore proposed that repetitive minor trauma to the shoulder predisposes to bacterial arrest in this area and thus development of infection. It is also proposed that the low weight and body mass index is likely to be a determinant in these patients having a reduced immunity to infection.
No grading system for septic arthritis has been published therefore a new grading system is proposed.
The outcomes of various operative methods for osteochondritis dissecans of the femoral condyles were reviewed, and choice of these operative methods were discussed.
Twenty-four cases (19 males and 5 females) which underwent operative treatments were reviewed. The operative methods included drilling, repositioning and fixation of the osteochodral fragment, and bone graft or osteochondral graft. The minimum follow-up period was two years. The medial femoral condyle was involved in 17 cases, and the lateral, in seven. Lateral discoid meniscus or meniscal injury was combined in all the 7 cases in the lateral. The operative methods were decided from the condition of the cartilage. Drilling was performed in cases with no or minimal cartilage damages (10 cases). Repositioning (if required) and fixation of the fragment using absorbable pins was carried out in cases with a partial or total fragmentation (7 cases). Bone graft or osteochondral graft was performed when the original site was already degenerated (7 cases). Partial meniscectomy was added when the meniscal injury was combined.
In patients who received drilling, the lesion healed radiographically in all the cases and they complained of no or minimal symptoms. In patients who received the fragment fixation, re-union of the fragment was observed in 71% and the clinical outcomes were satisfactory in most of the cases. In patients who received bone graft or osteochondral graft, although union of the graft was observed in all the cases radiographically, 71% of the patients complained of residual pain.
From the results, drilling is sufficient if the cartilage surface is not damaged. When the fragmentation occurred already, the fragment should be repositioned and fixed to the original site before degenerated, as its clinical symptoms were much better than those with bone graft or osteochondral graft.
The purpose of this study was to describe a clinical evaluation of the etiological factors in osteochondritis dissecans (OCD) of the knee from radiographic and arthroscopic findings.
Twenty-two knees of 20 patients (16 male and 4 female, 16.1 years old in average at surgery) with symptomatic OCD of the femoral condyle were studied.
The medial femoral condyles were affected in 16 knees of 14 patients (medial group) and the lateral femoral condyle in 6 knees of 6 patients (lateral group). These two groups were compared using radiological location and arthroscopic findings. In radiography, the location of OCD was classified in accordance with Cahill et al. (1989). On the anteroposterior view, five zones were numbered 1 to 5 from medial to lateral. On the lateral view, three zones were labeled A,B and C from anterior to posterior.
In the medial group, the locations of OCD were 23BC(12), 2BC(1), 23ABC(1) and 23C(2); 14(88%) of 16 knees involved in non-meniscal area. In the lateral group, the locations of OCD were 45C(4), 5C(1) and 4BC(1); 5(83%) of 6 knees involved in meniscal area. In arthroscopy the medial group did not have medial meniscal tear, while the lateral group had 5 lateral meniscal lesions of 6 knees; 3 discoid meniscus (2 with tear and 1 without tear), 2 bucket-handle type tear and one no meniscal lesion.
Lateral meniscal lesions (with or without discoid) might cause OCD of the lateral femoral condyle. In the medial femoral condyle, we thought that OCD did not relate to meniscal lesions.
The tension of a repaired rotator cuff was evaluated in nineteen patients who had a repair of a full thickness rotator cuff tear. The tension of the repaired cuff was measured at the operation using a simple spring scale. The tension was evaluated regarding the size of the tear, the duration of the symptom, the presence of trauma, and the post-operative results using a UCLA score. The average of the tension at the arm in 0, 30, and 60 degree elevations were 39.2±18.4N, 23.5±17.2N, and 14.2±13.4N respectively. The average tension of the patient who suffered from a trauma was 20.3±15.8N, whereas the one in the patients who had no history of trauma was 35.0 ±18.0N. The slight positive relation, not statistically significant, was found between the tension and the size of the tear. We could not find a significant relation between the tension and the range of motion or the muscle power in this study. The UCLA score was significantly higher in those patients who had less tension of a repaired rotator cuff. We have to be careful not to put too much tension on the rotator cuff when we repair it. Too much tension might damage the muscles and musclotendious units of the rotator cuff or fail to unite the cuff to the bone, resulting in dysfunction of the rotator cuff postoperatively. Then, how much is "too much"? Only a few papers have described the details of the tension of a repaired cuff. Our results show that the lower the UCLA score in patients with a higher tension of the repaired cuff. These results suggest that the tension of the repaired cuff, indeed, changes the results of a rotator cuff repair.
Anatomy of the rotator cuff tendons, their relationship to the greater tuberosity, and the tensile and compressive properties of the cuff tendons have been extensively studied recently. From these anatomical and biomechanical studies, it has been clarified that stress concentration at the anterior portion of the supraspinatus tendon, shearing force, and mechanical friction as well as the degenerative weakness of the cuff tendons can all play a role in the occurrence of a tear. Strength of initial repair is limited, and thus the arm after repair should be positioned such that undue tension at the repair site is eliminated.
Synovitis in the subacromial bursa (SAB) and the gle-nohumeral joint (GHJ) is often seen in rotator cuff diseases. In order to clarify its significance, following studies were conducted. The mRNA expression levels of IL-1B, sIL-1ra and icIL-1ra and the amount of substance P in the SAB synovium were correlated with the degree of shoulder pain. The cytokine-mRNAs in the GHJ synovium expressed more significantly in full-thickness tears (perforating tears) than in non-perforating tears. Biochemical markers (MMP-1, MMP-3) in the GHJ fluid were significantly higher in massive cuff tears than in smaller tears. These findings suggest the possibility that SAB and GHJ synovitis in rotator cuff diseases are associated with shoulder pain and the development of glenohumeral arthropathy, respectively.
In this histological study, the canine infraspinatus tendons were repaired to different bone surfaces: 1, a tendon end adjacent to the insertion: 2, a calcified fibro-cartilage layer; 3, a cancellous surface. Tendon repair to tendon ends restored the four-layered enthesis in the healing period, whereas tendon repair to the calcified fibrocartilage considerably delayed fiber development into bone. Fiber connection to cancellous surface developed according to the remodeling of trabecular bone by 12 to 16 postoperative weeks. Therefore, ruptured tendons should be attached to the remaining end or to a cancellous surface; they should not be attached to a calcified fibrocartilage layer.
To quantify the variation in strain between the deep and superficial layers of the supraspinatus tendon, ten cadaveric shoulders were tested on a purpose built rig. Differential Variable Reluctance Transducers (DVRTs) were inserted into the superficial and deep aspects of the tendon spanning the critical zone. DVRTs accurately measured linear displacement and from this strain was calculated.
The strain was measured for two aspects of supraspinatus action, abduction from 0 to 120 degrees with a tensile load (100 Newtons) and static load increases at zero abduction (20, 50, 100, 150 and 200 Newtons). After preconditioning, ten sets of results were recorded for each load/position.
The hypothesis, there is a statistically significant difference in strain between the superficial/deep supraspinatus tendon during abduction and with static loading, was tested using a one way ANOVA.
During abduction a statistically significant difference in strain was measured between the layers of the supraspinatus tendon at thirty degrees (p=0.000428) and this increased with further abduction.
Tensile loading increased tendon strain more in the deep layer of the tendon. This was statistically significant at loads greater than 150N (p= 0.007).
The variation in properties between the superficial and deep layers of the supraspinatus tendon has been proposed as a cause of differential strain (1). This study confirms statistically different strains between the superficial and deep tendon layers. It is proposed that the resulting shearing effect initiates intratendinous defects and ultimately tears.
Rotational acetabular osteotomy (RAO) is a circumacetabular osteotomy of the acetabulum designed to correct the dysplastic hip. In this procedure, the femoral head is covered with the articular cartilage of the acetabulum and the forces of weight-bearing are distributed more evenly. The purpose of this study was to determine whether RAO is effective in delaying the onset of arthrosis in patients with painful hip dysplasia.
We determined the outcome of 20 female patients in whom RAO was performed between 1975 and 1984; all were aged 20 to 29 years at the time of surgery. The pre-operative centre-edge angle of Wiberg was 0 or negative with proximal subluxation of the femoral head. Of these, 10 were lost to follow-up before the age of 42. In these patients, however, radiographs showed no signs of arthrosis at the last follow-up. The remaining 10 patients were examined 15 to 25 years after surgery, when they were 42 to 47 years old. Radiographs revealed findings of arthrosis in only two of them who had had the secondary acetabulum before surgery.
To evaluate the efficacy of preventive medicine, it is necessary to compare the results of intervention with the natural course of the disease. Wiberg reported on the natural history of seven female patients with severe hip dysplasia in 1939. When these patients were 13 to 34 years old, radiographs demonstrated no sign of arthrosis and the centre-edge angle was equal to or less than 12 degrees with proximal subluxation of the femoral head. These hips deteriorated to advanced arthrosis by the age of 42 years. Thus the outcome of our patients was significantly better than the natural course.
In conclusion, our study suggests that RAO is effective in delaying the onset of arthrosis in patients with painful hip dysplasia.
Surgical intervention is rarely indicated in the osteoporotic patient with compression fractures and kyphosis. In rare instances, the vertebral fracture is of the burst type, with spinal canal compromise and neurologic deficits, including paraplegia. These patients must be considered for surgical intervention. Reconstruction of such a spine poses technical challenges, because of concerns about adequacy of fixation and source of autogenous bone which is also osteoporotic. In addition, these patients frequently have serious medical conditions that increase the possibility of perioperative complications. Spinal shortening is a surgical procedure in which circumferential resection of vertebra is followed by closure of two adjacent vertebrae and fusion. It is mechanically more stable than augumentative spinal reconstruction and needs less bone graft.
Eight spinal shortenings were performed in eight patients for the treatment of paralysis due to osteoporotic vertebral collapse. Patients are ranged from 68 to 83 (average 74 years). Affected vertebrae were L1 in four, Th12 in three and Th9 in one case. After bone resection of affected vertebra from posteriorly through transpedicular route, shortening and correction of kyphosis was performed. Osteotomy was fixed by long segment instrumentation and short segment bone graft with Hartshill rectangular rod, sublaminar wiring and laminectomized local bone. Paraparesis which was present before surgery disappeared and spinal stability was obtained. Bony union was observed after six months. Surgical complication was seen in one case with hepatisis. A massive bleeding necessitating clamp of drain tube saved her life in the expense of neurological deterioration. We now consider this patient was out of indication for spinal shortening. With the follow-ups ranged from 9 to 36 months (average 19 months), neural function was preserved.
It was concluded that spinal shortening using instrumentation is a safe and effective procedure for the treatment of osteoporotic vertebral collapse with paralysis.
From 1996, we were added fenestration between coronoid fossa, and olecranon fossa at the time of debridement arthroplasty termed extensive debridement arthroplasty with medial and lateral approach.The purpose of this study is to investigate clinical results of extensive debridement arthroplasty.
17 cases could be followed more than two years. Their averaged age was 57.3 years old. Two elbows had a previous history of debridement arthroplasty. In preoperative averaged flexion angle was 105 and averaged extension was 28C Clinical evaluation was performed with the elbow score of Japanese Orthopedic Association Preoperative averaged JOA score was 54.6 points In ray study we investigated whether the fenestration was open or closed.
In all cases, their symptoms improved D All patients returned to their former occupations satisfied with the clinical results Infection postoperative fracture and ectopic ossification were not observed.The averaged JOA score was 91 points Postoperative averaged flexion was 127 averaged extention was 12_Improvement of extension was 16 and that of flexion was 22 Closure of the fenestration was observed in five elbows Osteophyte formations of the coronoid process and olecranon was seen in 4 elbows
The JOA score of pain and ROM of these results were superior compared with any reports of debridement arthroplasty.The JOA score and results of ROM were superior when the fenestration was open.To maintain the fenestration hole open some modification will be necessary
Short term results of extensive debridement arthroplasty showed satisfactory results in terms of pain relief and Improvement of ROM, especially in extension.
Patients with Lumbar Degenerative Kyphosis and Kyphoscoliosis (LDK) complain of stooped gait, persistent low back pain and weakness. Because operative treatment of LDK imposes considerable operative intervention for aged patients, an indication should be strictly limited; those have severe low back pain with lumbar kyphosis which afflicts upright walking disturbing house keeping, patients aged less than 70 as a rule and have no critical general complication as well. Purpose of this paper is to compare factors that affect the results of operative treatment of LDK.
19 patients were reviewed retrospectively in these series (av. aged 62.7, all female except one), who were followed-up for 3.0 years in average (14 months-8 years.) after the last surgery. Number of fused vertebra comprised 3 in 4 cases, 4 in 5, 5 in 3, 6 in 2, 7 in 2, 8 in 1, 9 in 2 respectively. In these cases 8 (av. aged 60.4) had no interbody fusion at all, one segment in one, 2 segments in 4, and 3 and more in 6 either anterior or posteriorly. Results were evaluated as excellent, good, fair and poor based on a correction rates of C7 plumb line and T1 tilt angle, as well as correction of lumbar kyphosis angle.
The result was evaluated as excellent in 2 cases, good in 6, fair in 6 poor in 5. No co-relation was found between the results and number of fused vertebra at the last stage. However, patients whose operation include interbody fusion (IBF) of 3 and more contiguous segments showed either excellent or good, but all cases with single segment or no IBF groop showed either poor or fair, where those with 2 segments had good in 2 cases and fair in 2 respectively. There were relatively many poor results due to instrument failures (6 cases), insufficient correction of the deformity, compression fracture and increase of kyphosis above and below IBF level, possibly caused by progression of osteoporosis and degeneration. Four patients were found nerve root symptom after surgery, but almost healed by revision in several weeks.
In order to obtain good result correction should include interbody fusion of at least 3 contiguous lumbar segments for multilevel anterior support and rigid instrumentation in sufficient length. Accurate planning before operation and careful surgical procedure should be emphasized to avoid nerve entrapment and instrument failure.
The role of spinal instrumentation in the presence of infection is still controversial, radical debridement of infected vertebrae and disc material may leave the spine unstable despite the use of bone graft, and some form of spinal stabilisation may deem necessary.
We reviewed 27 cases of primary pyogenic spinal infection treated in addition to an appropriate antimicrobial agents, by radical debridement, bone grafting and posterior (22) or anteror (5) spinal instrumentation.
The indication for surgery was the failure of conservative treatment (4), progressive neurological deficit (20) and the lack of diagnosis (3). The infection was caused by pyogenic bacteria (19), Mycobacterium Tuberculosis (6), Candida Albicans (1) Echinococcus granulosus (1).
The mean period of follow-up was 3.8 years (1–12). The infection was eradicated in all our patients, the neurological recovery was full in 19 out of 20 patients with neurological deficits.
Deep wound infection (Three immunocompromised patients, they all responded to repeated wound debridement); implant failure (Two patients, both required revision of fixation), early postoperative death due to nosocomial infection (1).
Spinal instrumentation may be indicated when after debridement and bone grafting, the stability of spine is compromised.
Since described by Kashiwagi in 1978, the Outerbridge - Kashiwagi procedure (OK procedure) has been used to treat osteoarthritis of the elbow when simple measures have failed. Despite being used for 20 years, there have been surprisingly few series. The aim of this study was to assess the medium to long term results of the OK procedure and to analyse the preoperative and operative findings to identify features which predict a good outcome.
A consecutive series of 43 patients (44 elbows) underwent ulnohumeral debridement (OK procedure) for osteoarthritis of the elbow. Their mean age was 57 years (range 24 – 85 years) with one female patient. 35 patients (36 elbows) were reviewed after a mean follow up of 39 months (range 12 – 71 months). Overall, 81% of patients were satisfied with 12 good, 19 fair and 5 poor outcomes. The mean arc of flexion/extension (p=0.001), pain score (p=0.002) and locking (p=0.003) were significantly improved but a significant number of patients developed rest pain (p< 0.0001). There was a complication rate of 17% (2 ulna nerve entrapment, 1 ulna nerve neuropraxia which resolved completely, 1 superficial wound infection, 1 wound haematoma and 1 myocardial infarction). The reoperation rate was 8% (2 revision OK procedures and 1 ulna nerve decompression).
Patients with symptoms for less than 2 years, considerable preoperative pain or cubital tunnel syndrome had a significantly increased chance of a good outcome. The absence of preoperative locking was associated with a significantly increased chance of a poor outcome. Joint space narrowing on radiographs or presence of posterior loose bodies at operation was associated with an increased chance of a good outcome but these were not statistically significant. A history of trauma, the preoperative range of movement and Xray score did not predict outcome.
The purpose of this study was to determine the significance of pedicular screw and segmental wire fixation for the treatment of spondylolysis.
Twenty-five patients of spondylolysis were treated operatively. Seventeen patients of them had isthmic sondylolisthesis with an average displacement of 22% (ranges, 4–55%). Thirteen patients (6 patients had spondylolisthesis) were treated by the direct repair of the pars defect with bone graft with pedicular screw and wire fixation methods (Group A), and 12 patients (11 patients had spondylolisthesis) were treated by posterior lumbar interbody fusion or postero-lateral fusion (Group B). The mean age at the operation was 34 in the former, and 45 in the latter. The average volume of bleeding was 291ml in Group A and 840ml in Group B. Operative results were evaluated as excellent, good, fair and poor by Henderson’s evaluation of functional capacity. Radiographically, bony fusion rate was examined. The average follow-up period was 33 months.
At the final follow-up stage, clinical outcome was excellent in 5 patients, good in 7, fair in 1, and poor in zero in Group A, and that was in 8,3,0, and one in Group B. Nerve roots irritation was observed in one patient in Group B postoperatively. Bony fusion rate was 100% in both groups. However, delayed union was observed in 2 cases of the Group A. The range of motion L5/sacrum increased to 10 degree from 9 degree (p=0.1)
Spondylolysis with severe low back pain has been treated by major surgery like spondylodesis. This study showed that the direct repair of the pars defects is the acceptable methods for the treatment of spondylolysis either no or minimal spondylolisthesis.
This is a study on the results of fifty consecutive patients who underwent endoscopic removal of herniated lumbar disc by interlaminar extra-dural approach. The indication for surgery was unrelenting, single level, unilateral sciatic pain not relieved by conservative treatment, with supportive evidence of disc herniation in MRI. Surgery was carried out in the lateral position. After localizing the disc space by X-ray, two 5 mm portals were made, one for an arthroscope and the other for working instruments. The spinal canal was entered through the inter-laminar route and under direct vision the herniated lumbar disc was removed.
The duration of study is from February 1998 to July 1999 with an average follow-up of 14.58 months. There were 31 herniated, 9 extruded and 10 sequestrated discs. All patients were mobilized the same day and 42 were discharged the next day. There were two patients who suffered partial but permanent nerve root damage, 4 had post-operative headache and one developed transient extra-pyramidal symptoms. Modified McNab criteria were applied to study the results by an independent observer.
40 patients (80%) had a very good outcome (i.e. fully functional with occasional discomfort); 5 patients were considered to have a good outcome (i.e. normal function with some restriction to strenuous activity); 2 patients who had partial nerve root damage were considered as fair results though their final outcome was good. 3 patients suffered recurrent disc herniation and were operated by open surgery. These were classified as failures. We conclude that this technique is a minimally invasive procedure with results comparable to conventional disc surgery. The advantages to the surgeon are the excellent illumination, magnification and visualization. The advantages to the patient are minimal surgical trauma and speedy recovery.
Eighty-two consecutive patients with forefoot pain and clinical signs strongly suggesting a neuroma all underwent ultrasound scan of both feet using a 10-5 MHz transducer where a well defined hypoechoic area defined a neuroma . All ultrasound positive feet had the lump excised surgically for histological studies. Plain x-rays were done on all symptomatic feet to exclude other pathology.
Sixty-four feet had an ultrasound positive diagnosis. Of these, there were 82.3% female and 17.1% male (ratio 4.8:1 , p< 0.001). Thirty-six percent had bilateral neuromata but with only one side being symptomatic.59.5% of the neuroma were located in the interspace between the third and fourth toes whilst 41.5% were found in the interspace between the second and third toes.
The size of the lesions varied from 3 to 11mm with a mean of 6.86mm. No lesion less than 5mm was symptomatic in our series.
One false positive was noted in the series giving the test a sensitivity of 97.9% but the specificity was low at 50% as the scan negative feet were not surgically explored for ethical reasons
All surgically explored patients had become asymptomatic at an average of 5.3 weeks (range 4–24 weeks) post surgery. Thirty-three ultrasound negative patients treated non-operatively were completely asymptomatic at an average of 30 weeks (range 6–50 weeks).
We conclude that an ultrasound scan is a cheap, non-invasive, time-efficient test useful in identifying interdigital neuroma as a cause of forefoot pain.
To evaluate the mechanism of dislocation of the navicular in complex foot trauma; we hypothesize this is similar to lunate/perilunate dislocations.
Our experience with 6 cases of total dislocation of navicular without fracture, and an analysis of 7 similar cases reported world-wide was used as the basis for this hypothesis. Radiographs of our patients and the published cases were analyzed in detail, and associated injuries/instablilities were assessed. The position of the dislocated navicular and the mechanism of trauma was considered and correlated, and this hypothesis was propounded.
When the navicular dislocates without fracture, it most frequently comes to lie medially, with superior or inferior displacement, depending upon the foot position at injury. It is hypothesized that the forefoot first dislocates laterally (perhaps transiently) at the naviculocunieform joint by an abduction injury; in all cases we recorded significant lateral injury (either cuboid fracture, or lateral midfoot dislocation). The relocating forefoot subsequently pushes the unstable navicular from the talonavicular joint, and depending upon the residual attachments of soft tissues, this bone comes to lie at different places medially. This is a similar mechanism to the lunate dislocation in the wrist, where the relocating carpus push the lunate volarly. Our clinical experience with these complex injuries has shown that the whole foot is extremely unstable. For reduction, the talonavicular joint has to be reduced first, and then the rest of the forefoot easily reduces on to the navicular. An understanding of injury mechanics allows us to primarily stabilize both the columns of the foot, and subsequent subluxation and associated residual pain are avoided.
Pure navicular dislocations are not isolated injuries, but are complex midfoot instabilities, and are similar to perilunate injuries of the wrist.
Motor vehicle accidents frequently cause injuries to the spine resulting in long term disability. The mechanisms of injury however, are poorly understood. Many of the currently available crash test dummies (e.g. EuroSid and Hybrid III) are deficient in consideration of the spine, lacking the correct biofidelic behaviour to accurately predict injury. We have developed a detailed mathematical model of the spine for the investigation of spinal kinematics and injury sustained during passenger vehicle impacts.
The model uses finite element analysis. Surface geometry was reconstructed using digitised co-ordinates from 6 vertebrae (T10 to L3) The location, geometry and physical properties of all 6 ligaments and the intervertebral discs were added. The model was extrapolated to represent the thoracolumbar spine. An independently developed model of the cervical spine was added. The LS-DYNA finite element analysis code was used for simulation of a wide range of non-linear dynamic scenarios. Simplifications of the model included replacement of deformable materials with rigid materials, replacement of complex joints with non-linear springs, and substitution of detailed ligament representations with springs and dampers. The complete spine model was then embedded into a dummy model (Hybrid III) to generate a realistic ‘crash loading’ on the spine.
The model has been validated against published data on stiffness, strength, range of motion, and known physical properties of individual functional spinal units. Further validation has been provided by data from volunteer and cadaveric testing. Loads representing a typical frontal impact were applied to the model. Ligamentous injury was predicted by monitoring forces and deflection within the model. The model accurately predicts bone stresses at which compressive wedge fractures, fractures of the pedicle and neural arch are known to occur.
A validated finite element model comprising 20,000 elements has been developed for analysis of spinal injury. The model accurately predicts ligamentous and bony failure. We hope the model will provide the basis for the development of casualty reducing design strategies within the automotive industry.
Giant Cell Tumour of the Tendon Sheath is a benign tumour of synovial origin most frequently affecting the upper limb. Up to 11% exhibit radiographic evidence of cortical erosion and intra-osseous expansion. In the upper limb recurrence rates of between 10–50% following excision have been reported. However, GCT-TS is rarely described in the foot and ankle and its behaviour is ill understood.
17 cases of this rarely described tumour in the foot and ankle are presented, describing their clinical presentation, histopathology, treatment and outcome.
Analysis of all cases of histopathologically proven GCT-TS of the foot and ankle from the Oxford Tumour Registry, was conducted between the periods of January 1984 to December 1999.
22 cases were identified of which 17 cases had adequate records to allow analysis of patient demographics, duration of symptoms, preoperative investigations, presumed diagnosis, precise site of origin, post operative complications and recurrence rates
The mean age of presentation was 28 (8–53). 10 cases were female and 7 male. 76% cases occurred in the foot, all of which arose adjacent to the phalanges or heads of the metatarsals. 14% occurred in relation to the ankle or sub-talar joint.
82% presented with a painless swelling. The duration of symptoms ranged from 6 months to 8 years. Only one patient complained of sensory symptoms.
Pre-operative investigations included radiographs in 64% with 3 cases having an additional MRI scan. The MRI scans of GCT-TS have characteristic changes on T1 and T2 images. The presumed preoperative diagnosis was incorrect in 82%.
36% of radiographs taken showed changes including cortical erosion and speckled calcification.
A local excision was performed in 15 cases, an amputation in one and a wide local excision in one case only. There have been no recurrences during the follow up period of between 1–12 years.
GCT-TS of foot and ankle is rare and is commonly misdiagnosed. Despite only a local excision being performed in more than 80% of this series there were no recurrences.
Plain radiographs may show cortical erosion or speckled calcification in up to 36% and MRI is helpful in further defining the anatomy of the lesion, allowing planned excision and reducing the risk of recurrence.
Between 1978 and 1999, surgical treatment for talocalcaneal coalitions which failed to respond to any conservative treatment was performed. Materials consisted of 46 patients (50 feet), including 26 males (29 feet) and 20 females (21 feet). The patients’ age at the time of operation ranged from 8 to 66 years (average, 22.5 years). Major symptoms included local pain (43 feet), tumor (19 feet), numbness of the plantar side (17 feet), peroneal muscle spasm (13 feet), and varus instability of the ankle (3 feet). Major signs included limited motion of the subtalar joint (50 feet), palpation of tumor (34 feet), sensory disturbance of the plantar side (14 feet), peroneal spastic flat foot (3 feet), and limited dorsiflexion of the ankle due to contracture of the gastrocnemius muscle (2 feet). The regions of the coalitions included middle type (36 feet), posterior type (9 feet), and diffuse type (3 feet). The coalitions were all incomplete unions, that is to say fibrous or cartilaginous unions.
Surgical treatments were as follows: coalitions were excised and subtalar joints were mobilized in 31, resections alone were carried out on 16, and 3 feet underwent arthrodesis of the subtalar joint. Results of surgical treatments were evaluated using our own clinical scoring system. 28 feet were excellent, 13 were good, 8 were fair, and one foot was poor.
In principle, the purpose of surgical treatment of these coalitions involved excising the tumor to release the plantar nerve from compression and resection the coalition to gain physiological subtalar motion. However, patients experiencing osteoarthrotic changes and whose coalitions occupy most of the subtalar joint should undergo an arthrodesis of the subtalar joint.
To investigate the limitation of proximal spherical metatarsal osteotomies for feet with severe hallux valgus, a follow-up study was performed on the patients whose preoperative hallux valgus angles were 40 degrees or more.
Forty-eight feet in 37 patients (11 male, 37 female, 60 years range 20 to 84 years) were investigated. Mean follow-up was 4 years and 1 month ranging from two to eight years. The spherical osteotomy, performed using a curved chisel, was devised for correcting not only varus deviation of the first metatarsal but also pronation and dorsiflexion. A distal soft tissue procedure was done at the same time. Twenty feet received combined operations for their combined deformities.
Eighty-one percent of the patients were satisfied with the results. However, six of twelve patients whose preoperative hallux valgus angles were 50 degrees or more were unsatisfactory. Mild metatarsalgia remained in eight feet at the follow-up, but no new metatarsalgia developed in any patients. The mean value of the hallux valgus angle improved from 46.6 degrees to 11.1 degrees. The patients whose preoperative hallux valgus angle were 50 degrees or more showed 16.4 degrees of average hallux valgus angle at follow-up. Their results varied widely and most of them had inadequate correction. The mean correction toward plantar flexion was 0.7 degrees. Average shortening of the first metatarsal was 3.4mm. The shortening of the first metatarsal had not caused worsening of metatarsalgia if adequate correction of hallux valgus was achieved and malunion toward dorsi-flexion was prevented.
The proximal spherical osteotomy could consistently achieve satisfactory results for the patients whose hallux valgus angles are under 50 degrees. However, the results were worse in feet with more severe deformities. Other procedures for hallux valgus or proper combined operations were necessary for such patients.
Numerous techniques of arthrodesis of the ankle have been described in the literature with variable results. Although arthrodesis achieves satisfying results in most cases, high complication rates have been reported. We utilized a medial compression T plate to achieve fusion and the aim of this study is to present the early to mid term results of this procedure at our institution.
20 patients (23 ankles) underwent ankle arthrodesis by a single surgeon using the same surgical technique. Under tourniquet control, a medial longitudinal incision centering on the medial malleolus was used. After osteotomising the medial malleolus to expose the ankle joint, chevron cuts were made in the tibia and the talus removing only enough bone. The cut surfaces are apposed and then compressed together by using a medial compression T plate. The excised medial malleolus was used as bone graft. The fixation was protected in a plaster cast and allowed only partial weight bearing for up to 10 weeks. The ankles were clinically assessed by Mazur ankle scoring system and radiologically assessed until fusion was solid.
The mean age at operation was 56 years (range 20–76) and the sex distribution was equal. Indication for surgery included either posttraumatic or rheumatoid arthritis. At a mean follow-up of 73 months (range 6–112), all the patients had complete pain relief. Complications included deep infection in two ankles (Rheumatoid patient, needed implant removal), subtalar pain in four and nonunion in one ankle. There was late loss of position in 2 ankles (same patient), who was later diagnosed with charcot’s joints. All the fusions occurred within 16 weeks.
The fusion rate with this technique was 96% with the medial T plate providing a stable internal fixation. Our experience suggests that medial compression arthrodesis of the ankle is a reliable and an easily reproducible technique with a very low incidence of complications.
To investigate the histological findings for a herniated cervical intervertebral disc that produces a high intensity signal on MR images.
Fifty-five herniated cervical intervertebral discs harvested from 49 patients were histologically and immunohistochemically examined. Herniated cervical intervertebral discs with a high intensity signal on axial T2 MR images were classified as a globular, linear, or mosaic type. The specimens were embedded with paraffin using standard procedures. Serial 4 μm thick cryostat sagittal sections were prepared for HE, toluidine blue, PAS, and Elastica van Gieson staining as well as immunohistochemical study. The monoclonal antibodies used were specific for human CD68, IL-1β, and TNF-α.
Preoperative axial T2 MR images indicated that 3 discs had no high intensity signal and 52 discs had a high intensity signal; 22 discs were globular, 20 were linear, and 10 were mosaic. Histopathologically, high intensity signal areas in globular discs consisted of nucleus pulposus surrounded by macrophages. These macrophages and the chondrocytes around them expressed IL-1β and TNF-α. Almost all of the patients with a globular disc, had had severe radicular pain. For the linear disc patients, the fissure was observed consistent with the high intensity signal. A substance that would produce positive results for PAS staining was rarely observed.
The current histological study suggests that a globular type of disc with a high intensity signal on an axial T2 MR image consisted of a nucleus pulposus. Results demonstrated that, in these herniated discs, infiltrated macrophages and chondrocytes expressed inflammatory cytokines, and these reactions were associated with radicular pain. In contrast, linear and mosaic discs showed no obvious substance corresponding with the high-intensity zone, but the fissure was observed. It appears that a high-intensity zone for a linear or mosaic type of disc suggested of a fluid-filled area and/or mucoid fluid.
Hallux rigidus is the second most common pathological condition of the first metatarsophalangeal joint, after hallux valgus. Manipulation of the joint and injection with steroid and local anaesthetic (MUA and Injection) is widely practiced, but the literature contains little information on the results of such treatment. We report the results of this procedure performed on thirty-seven joints, with a minimum follow-up of 1 year (mean 41.2 months). Patients with mild (Grade I) changes gained symptomatic relief for a mean of 6 months and only one third required further surgery. Two thirds of patients with moderate (Grade II) disease proceeded to open surgery. In advanced (Grade III) hallux rigidus little symptomatic relief was obtained and all patients required operative treatment. We recommend that joints are Graded before treatment and that MUA and injection be used only in early (Grades I and II) hallux rigidus.
Routine use of Computed Tomography (CT) to evaluate discogram morphology is time consuming, costly and incurs additional radiation hazards. In our spinal unit, discography is routinely performed without the aid of CT. Discogram morphology for different stages of disc degeneration is evaluated using the modified Adam’s grading system on images obtained on fluoroscopy. Our aims were to assess the validity of the modified Adam’s grading system of discogram morphology, by assessing its inter- and intra-observer agreement.
We reviewed the discographic images (133 intervertebral levels) of 71 patients with chronic low back pain undergoing discography as part of a preoperative assessment between 1995 and 1997. Using the modified Adam’s grading system, three independent surgeon observers of three levels of experience (Senior Fellow, Senior and Junior residents) retrospectively evaluated the morphological appearance of each disc level in a randomized and blinded manner. Each observer was supplied with descriptions and illustrations of the 5 grades1, and each level was classified accordingly. The exercise was repeated three weeks later. The respective inter- and intra-observer agreements were calculated using the kappa statistic (Fleiss 1971) and generalized kappa statistic (Landis and Koch 1977).
The inter-observer agreement was excellent (kappa = 0.77; standard error = 0.054). The intra-observer agreement for each of the three observers was also excellent (kappa = 0.8, 0.8, and 0.85 with respective standard errors = 0.046, 0.049 and 0.042).
Significance and conclusions: The inter- and intra-observer agreement and therefore the reliability of the modified Adam’s grading system is excellent. This classification is easy to apply and has a high degree of reproducibility amongst observers with different levels of spinal experience. In view of the high reproducibility, we recommend the Adam’s classification for the grading of discogram morphology. The routine use of computed tomography with the concomitant radiation exposure and additional cost would seem not to be justified.
Temporary immobilisation of joints can lead to permanent ankylosis or fusion. The aim of this study is to demonstrate that treatment of vertebral fractures by single level fusion and 2 level fixation preserves movement in the unfused lower motion segment after removal of metalwork.
12 consecutive thoracolumbar fractures were treated by posterior fixation over two motion segments with fusion of the upper injured segment. Average age 39 years (27–50yrs.) and 6 were male. L2 was most frequently affected (6) then T12 (3), L1(2) and L3(1). Using the Denis classification 9 were Burst type B, 1 was Burst type A and 2 were Compression type B. No patients had abnormal neurology or any other vertebral injury. All operations were performed by one surgeon (RC) within 7 days of injury. Metalwork bridging the injured vertebra was removed at mean 11 months (8–13 * one patient 27 months) and average follow up in this study was 12 months (2–40) after removal of metalwork. A simple pain questionnaire and flexion-extension radiographs were obtained. The average movement in the motion segment previously bridged by metalwork was 5 degrees (0–12). For comparison, the level below moved an average of 7 degrees (2–17). Kyphus angle was 11 degrees (1–18) on presentation corrected to 0 degrees at operation (−6 - +12) returning 1 year after removal of metalwork to 5 degrees (1–16). Pain scores (0–10) were measured retrospectively, prior to the accident mean 0(0–1) and at review 2.6 (0–6).
Only one patient failed to return to previous employment. She had the highest pain score at 6, showed no movement at the bridged motion segment where removal of metalwork was delayed to 27 months.
Many surgical approaches at decompression have been attempted for the thoracic outlet syndrome (TOS), but only the transaxillary and supraclavicular routes carry the best outcomes. More recently, a selective and tailored approach via the supraclavicular route has been favoured. We performed a retrospective review between 1978 and 1998, and report the outcome of the ‘’two surgeon approach’’ for TOS via the supraclavicular method.
An orthopaedic and vascular surgeon jointly conducted 30 operations for disabling symptoms relating to TOS in 27 patients (21F, 6M), mean age of 29 yrs (range 18–63 yrs), having performed the preoperative assessment in conjunction with a neurologist. In all cases, it was essential that patient selection for surgery was determined on clinical grounds rather than the presence of a cervical rib. Anterior scalenectomy was performed via the supraclavicular route except in one case where the infraclavicular route was utilised. Additional surgical procedures were carried out according to the underlying abnormalities, i.e. excision of cervical rib or band or medial scalenectomy. The first rib was always spared.
At mean follow-up of 37 mths (range 3-228 mths), 26/30 sides (87%) had excellent or good results. The results were fair or poor in three cases where scalenec-tomy alone was performed. There were no major complications and no patients required a re-operation. 24 patients (89%) returned to their previous lifestyle or occupation.
Our results suggest that, with a multidisciplinary assessment and two-surgeon team, good to excellent surgical outcomes can be achieved via the supraclavicular route without resection of the first rib. Instead of the current practise of routine transaxillary first rib resection, we recommend decompression via this approach with further procedures tailored to the abnormality identified.
In the 40 years since Smith and Robinson described the anterior approach to decompress and fuse the cervical spine, generally acceptable clinical results have been reported though few papers include any form of detailed outcome assessment. More recently Snyder and Bernhardt have described an anterolateral disc-preserving approach to treat cervical radiculopathy that does not entail vertebral artery exposure. We describe our experience of this procedure.
Surgery was performed on 40 patients ( 21 male, 19 female, mean age 41 years). Functional outcome was assessed by the Neck Disability Index (NDI), return to usual work status, patient subjective satisfaction rating, and by standard VAS. Radiographic evaluation was performed looking at the following parameters: neutral films – maintenance of interbody disc height/diameter ratio R and degree of kyphosis/lordosis: dynamic films – degree of movement maintained at operated motion segment.
At an average follow up of 20 months(range 6 – 36) the mean NDI had fallen from 45% to 10% .Mean neck pain score was 2 (pre op was 7), average arm pain score 1 (pre op was7). 93% of patients had returned to work, 85% to their original occupation at an average of 11 weeks. Patient satisfaction scores were: 85% very satisfied, 5 % satisfied, 5% unsatisfied and 5% very unsatisfied. Radiologically it was possible to preserve intervertebral body disc height and motion in some patients whilst others lost some height and motion. A minority fused spontaneously.
ACFID is associated with clinical functional outcome scores comparable with those reported in the literature for alternative procedures. Bone graft donor site morbidity is avoided and radiological results show that preservation of useful motion at the operated disc is possible.
We investigated clinical features and surgical outcomes for compressive cervical myelopathy in patients over 75 years of age.
Twenty-one patients who underwent surgical decompression for cervical myelopathy were reviewed. The average age at the time of operation was 78.0 years and the mean follow-up period was 5.7 years. Posterior decompression in 19 patients and anterior decompression in 2 patients were performed. Neurologic deficits before and after surgery were assessed using a scoring system by the Japanese Orthopaedic Association (JOA score). Radiological features were examined with radiographs and MRI. The clinical results were compared to those of 24 control patients who were less than 65 years of age at the time of surgery. The average age was 50.2 years and the mean follow-up period was 4.5 years.
In the aged patients, the preoperative mean JOA score was 6.2. Radiological examination revealed that the spinal cord was multisegmentally impinged. The postoperative maximum JOA score averaged 11.1, and the recovery rate was 45.4%. All patients became ambulatory and independent in fundamental daily activities following surgery. Maximum recovery was obtained from 1 to 3 years after the operation and function was maintained for at least 3 years. At the final follow up, the mean JOA score had been reduced to 9.5 and the recovery rate to 27.4%. Only the preoperative duration of symptoms correlated with the outcomes. The pre-operative JOA score in the control patients was 6.5. The postoperative maximum JOA score was 13.8 and the recovery rate was 69.4%. This was not significantly changed at the final follow-up.
Although postoperative recovery of function was significantly inferior to that of the control patients, surgical treatment appears to be beneficial, even in patients over 75 years of age, in improving neurological function and ability of activities in daily living.
Since 1982, 21 patients were operated at our hospital including 12 males and 9 females. The average age were 59.4 years, the average duration of HD was 15.5 years, and DSA was in the cervical spine in 14 cases, and the lumbar spine in 7. Symptoms were pain in 21 patients (100%) and neurological deficits in 19 (90%). Histological examination of respected specimen revealed amyloid deposits in all cases.
We classified the X-rays changes from DSA in stage 0 (no change) to stage 3 (end stage), and as type A (kyphosics), B (subluxation), C (amyloid deposits in soft tissues), and D (spontaneous fusion).
All 21 cases were classified as stage 3. The 14 cervical spine cases belonged to type A or B, but all 7 lumbar spine cases belonged to type C or were combined types.
In the 14 cervical spine cases, spinal fusion was done to stabilize the spine (AO plate in 3, Axis plate in 2, Olerud system in 2, and others in 7).
In contrast, posterior decompression (laminoplasty with or without spinal fusion) was done in all 7 lumbar spine cases.
The results were evaluated from the JOA scores. The score improved from 6.1 to 10.1 points (full score:17) in cervical patients and it improved from 12.2 to 20.2 points (full score:29) in lumbar patients. One patient died 2 days after surgery because of massive blood loss.
Twenty-one operations for DSA were investigated. Surgical strategies were decompression, stabilization, or combination. In addition, minimum invasive procedure should be considered for the patients with high-risk and the poor bone quality.
This is a prospective study assessing the results of patients receiving large fragment allograft and a vascularised fibular graft following primary malignant tumour resections around the hip and the knee.
18 patients underwent tumor resection followed by reconstruction with large fragment allograft and vascularised fibular graft. Eight patients underwent resection arthrodesis of the hip, four underwent resection arthrodesis of the knee and six underwent intercalary resections. Following tumour resection with adequate margins, an appropriate sized allograft fragment was internally fixed with either a plate or an intramedullary nail. A vascularised fibular graft was used to span the gap between the remaining host bones. Osteosarcoma was the commonest diagnosis. The patients were clinically assessed by MSTS functional scoring system and radiologically assessed at regular intervals.
The mean age was 26 years (range12–70) and majority of the patients was men. 11 patients received preoperative chemotherapy. Mean follow-up was 85 months (range 8–153). Six patients have died of metastatic disease at a mean of 33 months. Complications included local recurrence in two, deep infection in one and stress fracture of the fibula in two cases. One patient with local recurrence and the other with deep infection underwent an amputation. Majority of the patients had good or excellent MSTS scores at final follow-up and 75% of the patients are engaged in physically active occupations. Graft hypertrophy was evident in majority of the patients.
Our experience clearly indicates that reconstruction with large fragment allograft and vascularised fibular graft is a useful limb salvage procedure with the fibula hypertrophying slowly with time. The eventual fracture of the allograft or failure of the allograft-plate composite is to be expected but is not deleterious due to the physiological response of the vascularised fibula to the weight bearing stresses over time. We feel that this biological solution is likely to demonstrate superior long-term results compared to a prosthetic reconstruction.
To investigate the efficacy of the navigable intradiscal catheter in the treatment and relief of lumbar discogenic back pain.
Twenty-three (23) consecutive patients, at this site, were enrolled into the study by this investigator from normal practice. Inclusion criteria included presentation with predominant low back pain with or without referral leg pain lasting longer than 6 months, diagnosis of DDD or IDD confirmed by plain x-rays, MRI, and positive, low pressure discography, and failure of at least 6 weeks conservative treatment. Outcomes were assessed by clinical exam and administration of the SF-36 Health Survey during the baseline, 3, 6, and 12 month visits.
All treatments were performed on an outpatient basis. Following the administration of conscious sedation and local anesthetic, a 17-gauge introducer needle was placed by an extrapedicular approach into the symptomatic disc using fluoroscopic x-ray guidance. A navigable catheter was placed circumferentially to the posterior annular wall. Treatment time was 17 minutes at a maximum tissue temperature of approximately 90°C. Intradiscal antibiotics were employed post procedure and all patients were discharged the day of procedure without complications.
Thirty-three (33) lumbar discs were treated. Ten patients had single levels treated; thirteen had double levels treated. Twelve month results show significant improvements in pain as measured by a visual analogue scale (56% decrease, p = 0.035), and the SF-36 sub-scales measuring Bodily Pain (93% decrease, p = 0.011 at 6 months), Physical Functioning (65% increase, p = 0.035), and Role Physical (173% increase, p = 0.020). Overall, 80% of the patients were satisfied with their outcomes (p = 0.004).
The intradiscal navigable catheter has proven to be effective in the reduction of pain and an increase in functional abilities for patients who suffer discogenic low back pain due to IDD or DDD.
The purpose of this study is to call attention to the diagnosis of spinal cyst caused by lumbar disc herniation. Reviewing a total of 11 cases of lumbar spinal cyst that have been encountered in our spinal practice, we propose our views concerning the pathology of this lesion.
The clinical findings of lumbar spinal cyst are identical to those in acute disc herniation such as low back pain and radiculopathy. The characteristics of imaging study are as follows; The magnetic resonance imaging (MRI) demonstrates a relatively large, rounded mass postero-laterally to the vertebral body. These lesions are isointense relative to the intervertebral disc on T1-weighted images and homogeneously hyperintense on T2. A gadolinium -DTPA-enhanced MRI shows a rim-enhancing lesion. A discogram reveals leakage of the contrast medium into the mass.
The operative findings demonstrated encapsulated soft tissue masses which contained bloody fluid and small fragments of herniated disc tissue. The pathologic examinations revealed fibrous tissue with hemosiderin deposit in cyst wall and degenerative disc materials with inflammatory cell infiltration.
This type of lumbar spinal cyst has been recognized as spinal epidural hematoma in recent years. Wiltse suggested that epidural hematoma may result from tearing of fragile epidural veins due to acute disc disruption. However, MRI characteristics of hematoma are not identical with those with lumbar spinal cyst. It is more likely that the lesions showing the pattern of changes are herniated disc tissue accompanied by hemorrhage and inflammation. If hernial tissue is covered with some membranous susbtance, formation of cystic lesions is understandable. Hence, we hypothesize that lesions, in which lysis liquefaction and absorption of the herniated disc tissue associated with inflammatory response have progressed, and the herniated disc tissue has completely disappeared, may be filled solely with bloody fluid, showing an appearance like cysts.
Posterior approach to the lumbar spine necessarily induces structural damage of paravertebral muscles. In order to avoid these changes, we have started to utilize a microscopic decompression of the spinal canal via an unilateral approach since 1998. The purpose of this study was to evaluate the results of this operative procedure for lumbar spinal canal stenosis.
A total of 18 patients, 13 men and five women, were reviewed. The age at the time of surgery ranged from 53years to 78years with a mean of 69.0years. Follow up period averaged 12.3months ranging from one to 32months. As for operative procedure, unilateral paravertebral muscle was retracted laterally and lam-inotomy in the approached side was performed. Following complete decompression of a nerve root in the approached side, microscope was tilted and the inner aspect of lamina in the contralateral side was resected using high-speed drill with a guard of yellow ligament to dural sac and nerve root. Following the procedure, yellow ligament was resected and nerve root in the contralateral side was decompressed.
Results: In operation time, blood loss and recovery rate of JOA score, there were no statistical differences compared with ordinal laminotomy cases. Dural sac was well decompressed not only in the hemilaminec-tomy side but also in the contralateral side. All cases showed intensity change of paravertebral muscle in the approached side on T2 weighted MRI.
Conclusion: The procedure described here was definitely effective because paravertebral muscle in the contralateral side and midline structure of the lumbar spine could be completely preserved.
We assessed the usefulness of vascularized bone transfer for treatment of aggressive musculoskeletal tumours. Classification by reconstruction method with vascularized bone transfer of our 33 patients was made into five types: 1) intercalary type in 6 cases, 2) arthrodesis type in 5 cases, 3) arthroplasty type using fibular head in 8 cases, 4) hybrid type with recycling autograft as heat treated bone or irradiated bone in 4 cases, and 5) inlay type after curettage of benign tumour chiefly for femoral head and/or neck in 10 cases.
From October 1975 to December 1999, 33 patients composed of 18 males and 15 females with age ranging from 9 to 69 years (average of 30 years) received vascularized bone transfer. There were 28 cases of bone tumour and 5 cases of soft tissue tumour. In 31 cases we grafted the fibula of 8 to 20 cm in size and in 2 cases the ileum of 8 cm in size. Postoperative follow-up period ranged from 10 months to 15 years with average of 65 months.
Primary union was achieved in 31 cases postoperatively between 1.5 month and 4 months with average of 3 months. As complication, we observed fracture of the graft in 4 cases and local recurrence in 3 cases. Postoperative functional evaluation ranged from 33.3% to 96.7% with average of 76.7%. As for oncological therapeutic results, continuous disease free cases accounted for 27, case of no evidence of disease for 1, case alive with disease for 1, and cases of death of disease for 4.
Intercalary transfer of vascularized bone is best indicated for defect of long bone. Arthrodesis was performed in only one knee joint where reconstruction with prosthesis is usually indicated. In arthroplasty type, remodeling of fibular head was observed. In hybrid type, rapid bone union and low complication rate can be expected when compared to recycling autograft alone. In inlay type, femoral head necrosis even after wide curettage can be prevented.
To assess the clinical features, development of metastases, and survival rate of patients with local recurrence after the resection of osteosarcoma in a large series.
Five hundred and thirty (530) patients with high-grade osteosarcoma were treated between 1989 and 1998. Fifty-four patients (10%) developed local recurrence after resection and adjuvant chemotherapy. There were 38 men and 16 women with a mean age of 19 years (range 6–50). The mean follow up was 39 months (range 7–120 months). Forty-three patients (79%) had clear resection margins microscopically, while in 8 patients (15%) microscopic tumour was found at the resection margin, and contaminated excision was performed in 3 patients. Histological response was category 1 in 24% of the patients, and category 2 in 76%. Clinical features, treatment, and prognosis were analyzed. Survival rates were examined using Kaplan-Meier Analysis.
The average interval between the first resection and local recurrence was 15 months (range 2–109 months). Forty-one patients (76%) had local recurrence in deep soft tissue, 7 in bone, and 6 in subcutaneous tissue. Twenty-six patients (49%) had lung metastasis at the time of local recurrence, while 21 patients (38%) developed it later. Thirty patients (57%) were treated with resection of the recurrent lesion and 18 (32%) were treated with amputation. 1-, 3-, and 5-year survival rates after local recurrence were 0.57, 0.38, and 0.22 respectively.
87% of patients with local recurrence developed metastases either concurrently or at a later date. Immediate amputation did achieve local tumor control. However, the survival rate was not statistically higher. 87% of the local recurrence arose in soft tissue. Therefore, careful attention should be paid to secure the wide margin around biopsy tract, muscle insertion to the affected bone, and neurovascular bundle at the time of initial resection.
Chondrosarcoma is the second most common bone tumour and occurs in the third to sixth decades of life. It most commonly arises in the pelvis and proximal femur.
We performed a clinical, operative and histological review of all patients seen at our unit with chondro-sarcoma of the pelvis over a ten-year period. We iden-tified 36 cases of chondrosarcoma of the pelvis and a retrospective analysis of cases was performed examining the rate of tumour recurrence and mortality rate with respect to tumour grade, anatomical site and type of surgery performed.
25 patients had a primary tumour diagnosed, 6 tumours were secondary to MHE and the remaining 5 were recurrent tumours. The tumours were situated in the acetabulum (14), the pubic / ischial rami (7), and the iliac wing (15). Surgical procedures included wide local excision (18), wide local excision and total hip arthroplasty (4), hemipelvectomy and endoprosthesis (13), and hind quarter amputation (1). The median follow up period was 48 months.
10 year cumulative survival rate was 40% and poor survival was associated with iliac tumours and higher grade tumours. Mean time to recurrence was 18.5 months and cumulative 10 year recurrence rates were 44%. Increased recurrence was associated with iliac and rami tumours and those excised by local resection alone. High tumour grade was not associated with increased recurrence in our study. The overall surgical complication rate of the operative procedures was 27%. These included dislocation and infection of prosthesis. Conclusions: This disease continues to be a surgical challenge with a clear association between more radical surgery and low tumour recurrence rates. However this must be balanced against the potentially devastating complications associated with this major reconstructive surgery.
Due to advances in the assessment and treatment of patients with metastatic bone disease, the survival has improved in recent years.
It was the aim of this met-analysis to assess the outcome of patients with metastatic bone disease across Europe.
Five major bone tumour treatment centres participated in the met-analyses. Data had been collected prospectively and was retrieved from the databases for the purpose of this study. All patients were referred to the bone tumour centre for assessment and possible surgical treatment.
The data of almost 2500 patients were analysed. The average age at diagnosis was 60 years and the male to female ratio was 1:1.07.
The overall 5-year survival was 35%, but this was significantly better in metastatic disease of the thyroid and breast as well as multiple myeloma.
The number and site of metastases or the presence of a pathological fracture were not prognostic factors in terms of survival. Patients who were female or younger than 50 years of age at time of diagnosis had a better outcome.
This registry will be expanded and more information analysed to try and provide useful information about prognostic factors and outcome for patients with meta-static bone disease.
To identify if disease severity and cancer-risk might depend on genotype in Hereditary Multiple Exostoses (HME).
The discovery that the EXT family of tumour suppressor genes is responsible for Hereditary Multiple Exostoses (HME) now enables correlation of clinical features with genetic defects. Genetic epidemiological studies, such as this, may provide additional data of use to the clinician. In most population-based HME cohorts, the incidence of sarcomatous degeneration has been estimated as 1–5%. This is not high, but occurs at a younger age (on average 2–3 decades younger) than chondrosarcoma in the general population. Genetic stratification might allow a very high-risk subgroup to be identified, within which surveillance for neoplastic change in osteochondromas could be concentrated.
In a pilot study, 29 affected individuals from 17 families with HME were screened for EXT mutation, with mutations identified in 12 families. Pedigrees were obtained and a complete assessment of disease severity made. We have since expanded this cohort; a further 71 affected individuals from 34 families with HME have provided detailed pedigree data and undergone a simple clinical examination to assess number of palpable osteo-chondromas. EXT mutation was assessed by means of fluorescent single-strand conformational polymorphism (f-SSCP) screening, followed by sequencing analysis.
Validation of clinical examination : In those who underwent radiographic examination for clinical purposes, number of palpable osteochondromas correlated strongly with number seen on radiographs at 146 anatomical sites (r= 0.814, p<
0.001), validating the usefulness of clinical examination in a population analysis, and negating the need for a radiographic skeletal survey in individuals at risk from malignant change. EXT mutation : EXT mutation detection rates for f-SSCP were calculated to be 93%. As suggested in the pilot study, most (84%) were loss-of-function mutations. 60% had not previously been reported in the literature. There were 42 individuals with EXT1 and 29 with EXT2 mutations. Disease severity and EXT mutation: In the pilot study, median number of palpable osteochondromas were about twice as frequent in the 7 families with EXT1 mutation than in the 5 families with EXT2 mutation (p<
0.05). This was also reflected in overall disease severity scores. In the larger follow-up study, individuals with EXT1 mutation had a median number of 32 osteochondromas, compared with 16 osteochondromas in those with EXT2 mutation (Wilcoxon rank sum test p<
0.0005). Cancer risk: Six chondrosarcomas occurred, and were only found in individuals with EXT1 mutation.
The observation that osteochondromas are more frequent in patients with EXT1 than EXT2 mutations is an important message in genetic counselling. If disease severity and cancer risk is greater in individuals with EXT1 mutation, screening for neoplastic change might be targeted on this group, in which lifetime risk of malignant change in osteochondromas could be increased to between 5% and 10%.
Local recurrence (LR) following treatment of a sarcoma is generally accepted to be a poor prognostic sign and an indicator both of inadequate local control as well as of the failure of adjuvant treatment.
Of 2589 patients with non metastatic Ewings, osteo-sarcoma, chondrosarcoma or a soft tissue sarcoma, 316 have developed LR at some stage following initial treatment of their tumour. 120 were already known to have metastases elsewhere when they developed LR or were found to have them at time of restaging but 196 developed LR as the first sign of relapse.
The mean time to development of LR was 24 months and 72% had arisen within the first two years. Overall survival following LR was 25% at 5 years and 20% at 10 yrs. In patients with metastases at the time of LR or who were found to have them at the time of restaging the median survival was 6 months with only 12% being alive at 2 years. In those with LR as first sign of relapse median survival was 3 years with 30% long term survivors. Patients with low grade tumours had a better outcome than those with high grade – 50% being cured by further surgery. Of the high grade tumours without metastases at time of diagnosis relapsed Ewing’s had the worst prognosis with median survival of 8 months compared with 22 months for osteosarcoma, 36 months for STS and 36 months for chondrosarcoma, despite which overall survival was 16% for both Ewing’s and osteo-sarcoma patients but was 30% for chondrosarcoma and STS.
LR following sarcoma surgery is due to a combination of aggressive disease with inadequate surgery and ineffective adjuvant treatment. In isolated LR aggressive further treatment is justified with an outcome similar to that of metastatic disease.
Survival in the wake of hindquarter amputation and oncological treatment is improving; the hindquarter amputee population is increasing. Some amputees function well, others do not. To assess quality of life and function of hindquarter amputees.
21 amputees (10 females and 11 males) consented to take part in the study. Ethics approval was sought. Assessment was performed using postal questionnaires; SF36 for quality of life; TESS (Toronto Extremity Salvage Score) for physical function and mobility; IEFF( International Index for Erectile Function) for male sexual function; a prosthetics questionnaire to assess prosthetic use.
Mean age of the group was 55 with the mean survival of 7 years post amputation.
Quality of life results were compared to normal subjects and patients for long term illness. Amputees had a significant reduction in quality of life concerning physical function and pain. Social function, mental health and energy levels were equivalent to patients with long term illness.
The mean TESS result was 56.9 with females having a mean score of 61.7 and male of 48. 50% of the group considered themselves as severely to completely disabled; 50% considered themselves moderately disabled. Five were in full time employment.
Six males responded to the sexual function questionnaire. Impotence was universally experienced.
Only five amputees used their prosthesis regularly. All amputees have experienced and 20 continue to experience phantom pain.
This study illustrates that hind quarter amputees have poor physical function and a low quality of life. Phantom pain is universally experienced. Male amputees experience impotence. Addressing these areas would improve the life of current and future hind quarter amputees.
Tartrate-resistant acid phosphatase is contained in multinucleated giant cells of giant cell tumour of bone (GCT) and chondroblastoma (CBL) as well as in osteo-clasts. Yet few studies have so far been done regarding serum acid phosphatase (AcP) level in patients of GCT or CBL. The purpose of this study is to elucidate the clinical significance of serum AcP as a tumour marker for GCT and CBL. Serum AcP value was examined in nine GCT patients and three CBL patients before and after surgery. In the GCT cases, serum AcP values before surgery were high in five cases. They were 14.0 IU/L, 68.7 IU/L, 45.9 IU/L, 21.9 and 31.3 IU/L (normal value; 7.1–12.6 IU/L). They decreased after surgery to 7.7 IU/L (55% of the preoperative value), 8.2 IU/L (12%), 7.8 IU/L (17%), 6.1 IU/L (28%) and 10.0 IU/L (32%), respectively. Serum AcP values before surgery were within normal limits in the remaining four GCT cases. Even in these four cases, postoperative serum AcP level was lower than the preoperative level. Postoperative/preoperative AcP ratios in these four cases were 67%, 80%, 69% and 76%. In the CBL cases, serum AcP values were high in all cases. They were 15.1 IU/L, 13.1 IU/L and 13.7 IU/L. They decreased after surgery to 10.3 IU/L (68% of the pre-operative value), 10.2 IU/L (78%) and 9.7 IU/L (71%), respectively, all within normal limits. Therefore, it is concluded that serum AcP is a useful tumour marker for GCT and CBL in diagnosing the tumour as well as in evaluating the efficacy of treatment.
The aim of this study was to investigate the hypothesis that unicompartmental knee replacement (UKR) of a single arthritic tibio femoral compartment can slow the progression of arthritis to the other compartment.
All AP and lateral standing knee radiographs at entry and 8 years were scored using the Ahlbach scoring system. The Ahlbach system has been shown to have good inter and intra observer correlation, and to relate closely to pathological findings at operation. An intra and inter observer error study of our results confirmed good correlation.
In the UKR group, four out of 42 knees showed progression of a single Ahlbach grade (9.5%). 2 revisions for arthritic progression were added to this group making a total of six out of 42 (14.3%). In the control group 12 of the 42 knees progressed by one or two Ahlbach grades and a further case underwent surgery making a total of 13 (31%). This difference was significant (p< 0.01).
Conclusion: Recent studies have shown that with a better understanding of design, improved selection of patients and better surgical technique, a UKR can have at least as good, if not better, results than a TKR at 5 year follow up, and has benefits of preservation of anatomy, earlier rehabilitation, preservation of bone stock and easier revision. Our radiological findings in this study will need to be correlated with further randomised prospective clinical studies, but suggest that progression of Osteoarthritis is reduced by UKR, and that this should be an additional stated benefit of this surgical technique.
The aim of this study was to assess the value of plain AP and lateral radiographs in determining ACL condition in medial unicompartmental osteoarthritis.
Background: A functioning ACL has been shown to be important in the success of certain unicompartmental knee replacements. White (2001) has shown MRI to be too sensitive in this age group of patients. Keyes (1992) suggested that stress radiographs were necessary to accurately assess ACL integrity.
Method: One hundred and twenty-six patients undergoing knee arthroplasty for medial osteoarthritis, had their ACL’s graded as Normal, Frayed or Absent intra-operatively. Standard pre-operative AP and lateral standing radiographs were graded by the Ahlback system. On the lateral view, the plateau was divided into 5 zones from anterior to posterior. The zone, in which the point of deepest wear occurred, was recorded.
Results: There was a significant difference between the occurrence of deepest wear in the anterior three zones versus the posterior two zones for ACL normal and absent knees (2 = 46.85, P< 0.001). There was a significant difference between the occurrence of normal and absent ACL’s in Ahlback grades ≤3 versus ≥4 (2 = 53.8, P< 0.001). There was a moderately strong correlation between both zone of deepest wear on lateral radiograph and Ahlback grade with ACL condition (Spearman’s rho = 0.62 and 0.69 respectively). The Positive Predictive Values for the ACL being normal are 64% for Ahlback grades 3 or less and 67% for Zone of deepest wear in the anterior 3 zones. The Positive Predictive Values for the ACL being intact (but not necessarily normal) are 95% for Ahlback grade 3 or less; 91% for Zone of deepest wear in the anterior 3 zones; and 97% if these criteria are combined.
Combining Ahlback grade ≤3 with wear in the anterior 3 zones also gave a Negative Predictive Value of 92% for the ACL not being normal.
Conclusion: There is a “watershed” in ACL condition between Ahlback grade 3 and 4. Prostheses requiring Normal or Intact ACL’s should only be performed if Ahlback grade is ≤3. Standard radiographs can reliably predict ACL condition with high Positive and Negative predictive values.
The purpose of this study was to establish the long-term clinical outcome of the Oxford Medial Unicompartmental Knee Arthroplasty (UKA).
Methods: A continuous series of 420 patients underwent medial Oxford UKA. Indications were anteromedial osteoarthritis with full thickness lateral compartment cartilage, a functioning anterior cruciate ligament and correctable varus deformity. Survival analysis with all cause revision as the endpoint was carried out for the entire group. At the time of this study 121 were still alive at 10 years and pre/post-operative 10-year clinical data had been prospectively recorded for them from which the AKS and HSS scores were calculated. Results: Seventeen patients required revision (4%) and the fifteen year survival rate was 94.3% (95% CI 85.6 - 100%). At ten years AKS and HSS scores were: AKSS (Knee) pre 30 / post 90, AKSS (Function): pre 42/ post 69 and HSS pre 56/ post 86. The differences were statistically significant (p< 0.01).
Discussion and Conclusion: We conclude that providing careful patient selection is maintained, meniscal bearing medial unicompartmental knee arthroplasty has clinical and survival results comparable to modern total knee arthroplasty. The advantages of lower morbidity and earlier return to function, enhanced by the introduction of minimally invasive techniques may make this the treatment of choice for suitable patients with anteromedial osteoarthritis of the knee.
Introduction: The Oxford medial unicompartmental arthroplasty (UCA) is now routinely performed through a short incision without Dislocation of the patella. The aim of this study was to assess the one-year results of this new technique to determine whether it enhances the quality of outcome, as well as the speed of its achievement.
Method: The first 88 consecutive Oxford UCA’s (Phase 3) implanted into 75 patients by two consultant surgeons were scored pre-operatively and at review with the American Knee Society Score. The average age of the patients was 68.1 years; the male to female ratio was 0.9 to 1.
Results: At review, one patient (one knee) had died and one knee had been revised for infection. The other patients (86 knees) were examined at a mean of 1.3 years from surgery. The average ‘knee score’ improved from 37 points to 95 and the average ‘functional score’ from 51 points to 93. Average maximum flexion improved from 117° to 132°. The ‘knee score’ outcome categories at review were 87% excellent, 8% good, 2.5% fair and 2.5% poor.
A randomised controlled trial was performed to compare the clinical outcome for the two commonest types of anterior cruciate ligament (ACL) reconstruction. Methods: Patients undergoing elective anterior cruciate reconstruction were randomised into one of two groups. Group PT underwent reconstruction using a patella tendon autograft (n=14), whereas Group SG had a semitendinosus/gracilis autograft (n=18). The same surgeon performed all operations. IKDC self reported function and activity scores were recorded pre-operatively and at one and five years post operation. KT1000 values and muscle strength were recorded pre-operatively and one year post operation.
Results: No significant difference between groups was found for any measurement at one year despite adequate study power. At five year follow up patients in the PT group had superior scores in every category of the IKDC self reported function score (mean IKDC score for PT group = 83, mean IKDC score for SG = 75). The activities of squatting and kneeling revealed the greatest difference between groups. It was found that 71% of patients in the PT group achieved IKDC scores of 80 or over whereas only 61% of patients in the SG group achieved 1 KDC scores of 80 or over.
Twenty four operations were reviewed in 23 patients to show a modified Roux-Goldthwait operation would improve the symptoms of chronic patella instability. This retrospective study used a questionnaire to record symptoms before and after surgery. The examination assessed joint hypermobility, patella tracking and stability, the Q and valgus angles of the knee. Apprehension test and assessment of patella tilt was also assessed. All patients underwent radiographic assessment. Twenty of 23 patients were improved by this procedure. Patella subluxation was reduced by 22%. Patella dislocation was reduced by 86%. The 3 unsuccessful cases had generalised joint laxity and may have been improved by the addition of a medial reefing procedure. There were no cases of tibial tuberosity numbness post operatively, patella tilt or failure of the transposed tendon. We showed that this procedure is effective, regardless of x-ray signs. We did observe a subjective increase in patellofemoral pain post operatively.
We fatigue-tested a new resorbable composite screw (PLLA/tri-calcium phosphate) and a metal interference screw. We present average data and tolerance limits.
Means and standard deviations of pullout strength were compared. Log-log curves were fitted between force level and cycles to failure. LTLs were calculated.
The aim of this study was to assess the distribution of wear down to bone in lateral compartment osteoarthritis and to analyse the effect of ACL condition and Ahlbach grading on this distribution.
Background: The distribution of medial compartment wear is now well described and shows posterior progression and increased area of wear with worsening AhIback grade and ACL condition (Porteous 2000). Harman (1998) described wear situated more posteriorly in the lateral compartment but did not show any change to this with altering ACL function, and did not assess the severity of the arthritis.
Method: Forty two tibial plateaus resected at total or unicompartmental replacement for lateral compartment osteoarthritis were analysed for the anterior and posterior extent of wear, as well as the point of deepest wear and the size of lesion. The plateau was divided into five zones from anterior to posterior. The ACL condition at surgery was graded as Normal, Frayed or Absent. Radiographs were classified by Ahlbach grade. Analysis using Mann-Whitney U-test, Fisher’s exact test and Spearman’s rank correlation were performed.
Results: The significant changes with increasing Ahlbach grade were that: the point of deepest wear moved posteriorly, the posterior extent of wear moved posteriorly and the size of the lesion increased. With ACL deterioration and rupture, the anterior extent of the wear moved forward and the size of lesion increased, but this did not occur through posterior migration of the posterior extent of the wear. There was a significant difference between the Ahlbach grade of ACL Normal and Absent knees.
The aim of this study was to report our experience of patellofemoral arthroplasty in isolated osteoarthrosis.
Material and Methods: The Lubinus Patellofemoral Arthroplasty was performed between 1989 and 1995 in 76 knees. The Avon Patella Femoral Arthroplasty was used from 1996 to 2001 in 187 knees. The average age of the patients was 65.5 years (range 36–87) with a male to female ratio of 1: 5. All the patients have been prospectively reviewed with standard radiographs, the Bristol Knee Score, and more recently Bartlett and Oxford scores.
The Avon Arthroplasty with improved design features for better tracking and congruity was introduced in 1996 and 187 have now been inserted in 147 patients. One hundred and nine knees have been followed for 8 months and 82 have completed the 2 year follow-up. Two patients have undergone revision to a TKR 97.5% (survivorship 2 out of 82). Three patients have had a unicompartmental arthroplasty added for disease progression. There have been no cases of patella maltracking or subliaxation.
Four year survivorship for moderate pain and revision is 96% (79 out of 82). Functional scores compared favourably with parallel series of total knee replacements.
Conclusion: The medium-term results of the Lubinus Patello Femoral Arthroplasty are unsatisfactory. We suggest the use of this prosthesis should be discontinued. The Avon Arthroplasty has improved results in the short-term.
The purpose of this study was to determine the rate of polyethylene wear in a fixed bearing knee replacement in order to establish a norm against which mobile bearing implants can be judged.
Linear wear was measured using an electronic micrometer and volumetric wear by creating a mould of the defect using dental wax, and subsequently weighing the wax.
Results: All components developed dishing which varied in orientation but matched the alignment of the femoral component. A near congruous articulation was thus produced correctly aligned for that particular arthroplasty. The mean linear penetrative wear for the group was 0.33mm (0.09mm per year) and the volumetric wear 124mm³ (26mm³ per year). The rate of wear seemed greatest during the second year.
Schuss radiographs are PA weight bearing views of the knee taken in 30 degrees of flexion. They are more sensitive detectors of osteoarthritic changes in the knee than standard extension AP views.
Aim of this study was to determine whether the increased severity of degenerate change shown on these radiographs is sufficient to alter proposed orthopaedic management of patients.
Methods: fifty consecutive patients aged 45–75 presenting to clinic with symptoms suggestive of tibiofemoral osteoarthritis were included. Each underwent standard clinical assessment and weight bearing extension AP and lateral radiographs of the knee. In addition a digital photograph of the legs and a single schuss radiograph were taken. This information was collated onto slides, two per patient. One slide included the history and examination findings plus the photograph, extension AP and lateral radiographs. The other was identical save that the extension AP was replaced by the schuss radiograph. The slides were randomised and shown to eight consultant orthopaedic surgeons. For each slide each consultant was asked to give his preferred management. Responses for the two slides of each patient were compared.
Results: The panel changed their management plan in over 40% of cases. This represented a reduction of almost 50% in arthroscopies in the schuss group with a move towards definitive surgery. Total number of procedures proposed was also reduced.
Introduction: Traditionally adolescent anterior knee pain is considered to be a self limiting condition with no long term sequelae. However recently two publications have suggested the condition may be longer lasting. We wish to suggest that adolescent anterior knee pain may lead to patello femoral arthritis.
All patients were sent a postal questionnaire enquiring about adolescent anterior knee pain, knee injury and patella instability.
Results: Ninety-three PFR patients and 86 UKR patients replied. The incidence of adolescent AKF and patella instability was higher in the PFR.group.
Review of 133 cases of Anterior Cruciate Ligament (ACL) reconstruction, showed 91 cases had been arthroscoped twice. The incidence of meniscus pathology, at first arthroscopy was 71% and this fell to 63% at the second arthroscopy and reconstruction. 21% of recurrent tears were in previously undamaged menisci. The medial meniscus, was the most commonly damaged meniscus, at the time of the first arthroscopy. The incidence of lateral and bilateral meniscus pathology increased in the time period awaiting ACL reconstruction. The mean time between the two arthroscopies were 27 months. Damaged menisci continued to tear over the time period between first and second arthroscopies or new pathology occurred. The paper concludes that if ACL reconstruction is performed by a mini open technique then it should be re-arthroscoped immediately before the ACL reconstruction. This is essential to avoid missing meniscus pathology, even in previously arthroscoped knees.
Imaging techniques including MR scanning and ultrasound were discussed. However it was noted that for standard orthopaedic practice in the UK plain films were the initial imaging available. The importance of taking a skyline view was stressed.
The Dejour protocol was then outlined where the lateral Xray of the knee assesses the patellar height, the presence of dysplasia of the trochlear groove, and, if present, its boss height. A CT scan defines the patellar tilt angle, and with cuts through the tibial tubercle, the offset of the tibial tubercle from the trochlear groove (TTTG). The four abnormalities that can be defined are then corrected at operation. All patients undergo a lateral release. If the patellar tilt angle is greater than 20° then a medial reefing is performed. If the patellar height is greater than 1.2, a distalisation of the tibial tubercle to correct this to 1.0 is done. A MG of greater than 2Omm leads to a correction by an Elmsie medial tubercle transfer. A boss height of greater than 6mm suggests a trochleoplasty should be performed. However the Dejour protocol is yet to be validated.
It was concluded that imaging is essential for analysing patellofemoral instability. Plain films alone do not give enough information. Patterns of patellofemoral instability as assessed by CT scan (and MRI scan) are yet to be established. Postoperative imaging to confirm correction of abnormalities should be done. The measurements are worthwhile but their validation is awaited.
The purpose of this study was to evaluate the role of high tibial osteotomy (HTO) [Lateral closed wedge v/s medial open wedge] in varus aligned knees with ligament instability. (ACL, PCL, PLRl).
We treated 14 patients with knee instability and varus alignment with HTO with or without ligament reconstruction. 5 patients with varus angulated ACL deficiency (double varus) were treated with single stage closed wedge HTO and ACL reconstruction. Of the remaining nine patients with PCL + PLRI injuries with varus angulation (Triple varus), six were treated with LARS ligament reconstruction with HTO, and the remaining were treated with HTO without ligament reconstruction. Four of these patients with triple varus had a open wedge HTO and the remaining five patients had a closed wedge HTO.
The mean time interval between injury and index surgery was 8.3 years. At a mean follow-up of 2.8 years 12 knees (86%) were stable and eliminated of giving way. In one patient the result was compromised with severe infection. Five patients (35%) continued to have varying degree of pain. According to the Cincinnati knee scoring system there were eight good, four fair and two poor results. In patients with triple varus, open wedge HTO had better scores than closed wedge HTO.
The results of this series are encouraging and we recommend HTO with ligament reconstruction in these complex cases.
A radiological and histological analysis of five knee joints after a minimum of 15 years following the implanting of carbon fibre which had been used as a treatment for knee instability was undertaken. All patients underwent Total Knee replacement for secondary osteoarthritis. Histological analysis demonstrated a variable amount of macroscopically visible carbon particles in the synovium, hyaline cartilage and menisci showed . At microscopy these particles were found enveloped by giant cells and lying quiescent with no active inflammatory changes. No intact carbon fibre ligament was noted within the joint, small portion of the old ligament were covered with a thin fibrous layer but there was no evidence of any structure resembling neo-ligament.
Extra articularly the carbon fibre was covered with a thick fibrous sheath with no active inflammatory changes inflammation. In the bone tunnels the carbon fibre- bone interface showed an apposition of the bone to the carbon fibre without any interposing fibrous sheath.
The histology suggests that carbon fibre bonds directly with the bone without fibrous interposition and that there is no evidence of synovitis changes related to the carbon fibre material.
The study suggest that although carbon fibre failed structurally as a ligament replacement it did not cause any significant long term inflammatory pathology.
The purpose of this study was to assess if the use of sterile stockings in lower limb surgery results in the contamination of the operative site with skin commensals from unprepared skin.
Twenty-five consecutive patients under going elective single knee arthroscopy were included in our study. All patients were operated on in the same laminar airflow theatre, by the same surgeon using the same method of skin preparation and operative technique.
Skin swabs were taken from each patient’s foot prior to the commencement of surgery. The limb was then prepared as follows;
An unscrubbed assistant holds up the leg, the leg is then prepared with betadine, by the surgeon from ankle to thigh, sparing the foot. The surgeon then towels off the thigh. The surgeon with the stocking in his hand, then takes hold of the foot using the stocking and unrolls it over the foot and up the leg. The stocking is bandaged in place and surgery commences.
Two samples were also cut from the cuff of the stocking, one prior to its use to act as a control and the other once it had been unrolled up the leg. The three samples were then sent to microbiology. The swabs were plated out on blood (x2), chocolate and Maconkey agar. One blood plate was incubated anaerobically at 37°c and the others in air at the same temperature. The stocking sample was cultured in nutrient broth. After 48 hours isolates were identified using standard techniques.
The results showed that none of the stocking samples yielded positive microbiology, however all of the foot swab samples did. They all grew coagulase negative Staphylococcus (CNS), five also grew conforms and one grew Pseudomonas, as well.
We can conclude from this, that this method of skin preparation using the sterile stocking is safe. It appears in this study, that the action of unrolling the stocking over the unprepared foot and then up the prepared leg does not contaminate the prepared operative site with commensals from the foot. However concern is raised by the high incidence of CNS on the foot, and may be a source of potential infection.
Introduction: We performed a prospective double blind randomised clinical trial to measure the effect of pre-operative infiltration of local anaesthetic around arthroscopy wounds compared to post-operative infiltration on post operative pain relief. The underlying clinical principle is for therapeutic intervention to be made in advance of the pain rather than as a reaction to it.
Methods: 36 patients undergoing daycase unilateral knee arthroscopy between October 2000 and March 2001 were studied. The pre-operative group had 10ml 0.25% bupivicaine infiltrated around the arthroscopy portal site following induction of general anaesthesia (G.A.), the postoperative group received 10ml 0.25% bupivicaine after the procedure but before reversal of the G.A. Pain was assessed using a 10cm Visual Analogue Score (VAS) at pre-operative, 1, 2 and 24 hours post operative. At each assessment the patients were blinded to the previous scores that they had submitted. Oral analgesic use in the post-operative 24 hours was also recorded.
At 1 hour post-op the mean VAS in the post-op group was 1.58 and in the pre-op group 2.59. This difference was not statistically significant (p=0.18).
The mean VAS at 2 hours post-op in the pre-op, group was 1.76 compared to 1.82 in the post-op group. This difference was not statistically significant (p=0.9932).
At 24 hours the pre-op group had a lower mean VAS (2.25) than the post-op group (2.4). This difference was however not statistically significant (p=0.7418).
Analysis of the post-operative analgesia requirement in both groups failed no reveal a statistically significant difference (p=0.3965).
Conclusion: In daycase knee arthroscopy under general anaesthesia there is no beneficial role in the use of pre-emptive local anaesthetic infiltration around the arthroscopy portal sites as compared to post-operative infiltration.
The aim of this study was to analyse the kneeling ability of patients before and at one and two years after total (TKR), unicompartmental (UKR) and selective patellofemoral (PFR) knee arthroplasty, for osteoarthritis. Method: Data was prospectively collected on 253 knees, which underwent either TKR, UKR or PFR. A kneeling score was obtained by analysis of the relevant section of the Oxford Knee Score questionnaire. Scores were obtained pre-operatively and at 1 and 2 years post-operatively (minimum score 0, maximum 4). Absolute values and change following arthroplasty were recorded. Correlations with pain and other knee functions were also made.
Results: Kneeling ability prior to surgery was poor in all three groups (mean score 0.7 out of 4) and improved significantly after surgery (mean score at one year 1.13 and at two years 1.46 out of 4) (P< 0.001). Kneeling ability at 1 year differed significantly with operation type (p = 0.02). Kneeling ability improved most in the first year post-operatively but continued to improve between one and two years although the final function was still not good. Kneeling ability was best in UKR and worst in PFR, with the difference between these prostheses being statistically significant (P< 0.001).
The aim of this study was to demonstrate the effectiveness of a customised coupled arthrodesis nail.
Knee arthrodesis is now infrequently performed and is usually reserved as a salvage for infected Joint arthroplasty or occasionally for intractable pain. Many methods have been used. Recently locked intramedullary coupled nails have gained in popularity. To deal with all size combinations a large inventory is required. We wish to report our series using a customised implant and to compare the outcome with other methods of knee arthrodesis.
Nine patients underwent arthrodesis using this implant, six following infected arthroplasty, two for intractable anterior knee pain and following trauma. Comparison was made with 17 arthrodeses performed since 1993 using external fixation (8), plates (4), and long K-nails (5). Union was achieved in nine patients (100%) at a mean time of 10 months using the customised implant. There were no complications despite early weight-bearing. No further procedures were required. This contrasted with a union rate of 65% with a 76% complication rate using alternative techniques. Seventy six percent of this second group required a further operative procedure.
We conclude that a customised coupled intramedullary nail can give excellent stability allowing early weight-bearing, and results in a high union rate with minimal post-operative complications. The differences in need for further surgery and occurrence of complications were statistically significant (p< 0.001), and differences in in-patient stay and non-union rate were also significant (p< 0.05) using Fisher’s exact test.
The aim of this study was to determine prospectively whether a lateral capsular approach to the knee joint for the purposes of total knee arthroplasty confers any advantage over the traditional medial capsular approach.
One hundred consecutive valgus osteoarthritic knees with greater than 10′ deformity were randomised into two groups each using a different surgical approach to the knee joint but all patients receiving the same type of arthroplasty components. One group had the replacement arthroplasty utilising a standard medial para-patellar approach and incorporating a lateral retinacular release where required whilst the other group received a modified lateral capsular approach avoiding osteotomy of the tibial tubercle and repositioning vastus lateralis at closure. Both groups were well matched in terms of age and sex. Each patient was reviewed in a special clinic at one year post-op to establish functional outcome and to review post-operative complications and length of stay and to conduct a radiological assessment of the implant. Pre and post-operative assessment utilised the HSS and Oxford knee scores. The assessor (a research physiotherapist) was blinded to the randomisation.
Results: All one hundred patients will have had their twelve month follow-up by February 2002. The results of the first 67 knees have been analysed in a preliminary study. The knee post-operative HSS and Oxford scores for the medial capsular group were 77.4 and 26 respectively and for the lateral capsular group 81.2 and 26.8. 79.4% of the patients in the medial group and 88% of patients in the lateral group showed good to excellent results on HSS scoring. Average patient satisfaction on a scale of 10 was 7.9 for the medial group and 8.5 for the lateral group. Other criteria such as range of motion, correction of deformity and stability were comparable in the two groups but it was noted that there was a tendency to use more constrained implants in the medial group. The differences between the two sets of results are not statistically significant in this preliminary report. There was no increase in wound complications in the lateral group despite incomplete closure of the capsule.
Introduction: In conjunction with a bilateral randomised control trial comparing the clinical outcome of two total knee arthroplasties (TKA), we carried out an in-vivo fluoroscopic analysis of both knees in the trial. Knee A, is a new mobile bearing posterior cruciate retaining TKA and Knee B, an established fixed bearing posterior cruciate retaining TKA.
Method: In an ethically approved study, video fluoroscopy was taken of both knees of seven patients performing three exercises; extension against gravity, flexion against gravity and a step up exercise. Ten images at ten-degree intervals over the flexion range were frame grabbed and digitised. The relationship of patella tendon angle (PTA) to knee flexion angle (KFA) was assessed using a newly developed computer system. Five normal knees in fit volunteers were also fluoroscoped and assessed.
Results: A similar pattern of results was obtai ed for all three exercises. Knee A behaved in a linear, more consistent fashion than Knee B, which behaved non-linearly. Analysis of variance showed this difference was significant for all three exercises (p < 0.039).
The aim of this study was to demonstrate the benefits of a simple blood transfusion protocol in Primary Total Knee Replacement.
Patients undergoing TKR in the UK usually have either blood cross matched or have an auto transfusion of drained blood postoperatively. Audit of blood requirements of patients undergoing TKR showed that a large amount of blood was wasted. A CT ratio (Ratio of number of units of blood cross matched to number of units transfused) of 4.86 was obtained. Range recommended by the blood transfusion society is 2: 1 to 3: 1. A protocol was then made to Group and Save and Antibody Screen for all patients having a primary TKR, except patients with haemoglobin less than 12.5 gm/dl pre operatively and those patients with multiple red cell antibodies in their blood.
A further study involving 50 patients was carried out using the new protocol. Two units of blood was cross matched for each of 5 patients (3 with Hb < 12 gm/dl and 2 with red cell antibodies). Post operatively the 3 patients with Hb < 12 gm/dl required blood transfusion of 2 units each, reducing the CT ratio to 1.7: 1.
The benefits from above protocol are : a). Patient safety as risks of transfusion are avoided and b). Cost saving for trust on haematology technician time and on transfusion sets which cost around £70 each.
Our study aims were to establish correlations between the incidence of patellofemoral pain and clinical, functional and radiographic outcomes in Total Knee Arthroplasty (TKR), using the Duracon prosthesis without patella resurfacing.
A consecutive cohort of 52 patients (71 knees) were reviewed at a special follow up clinic at a mean of 29 months. All operations were carried out by a single surgeon or under his direct supervision using a standard procedure. Patients were evaluated clinically and asked directly if they had anterior knee pain. American Knee Society Scores (AKSS) and knee alignment were assessed and patients completed SF-12 and WOMAC questionnaires. Standardised 45 degree skyline and standing lateral radiographs were taken and assessed by a single blinded observer, and patella tilt and displacement measured using Gomes’ method, and patella height measured using the Insall-Salvati ratio. Knees with patellofemoral pain underwent triple phase bone scintigraphy using Technetium 99m-MDP with vascular, blood pool and static (3 hour) imaging.
Significant patellofemoral pain was identified in 8 knees (11%), in 6 patients. This group had a reduced mean AKSS compared to knees without patellofemoral pain, although 50% still had a good to excellent outcome as judged by the AKSS. Only 2 knees with patellofemoral pain had abnormal alignment (2 and 12 degrees valgus). The mean SF-12 and WOMAC scores did not differ significantly between knees with patellofemoral pain and those without. Patella tilt and displacement were a common finding in this cohort, and could be as great as 17 degrees and 30% respectively without patellofemoral dysfunction. Paradoxically the mean values for these parameters were found to be reduced in knees with patellofemoral pain. Patella height did not substantially vary between knees with patellofemoral pain and those without. Bone scintigraphy of 7 of the knees with patellofemoral pain revealed a spectrum of activity from complete normality (3 knees) to tricompartmental increase in activity (2 knees). Increased activity localised to the patellofemoral articulation was evident in 2 knees.
We conclude that despite favourable overall results, the Duracon prosthesis fails to eliminate patellofemoral pain without patella resurfacing. This conflicts with excellent reported results using this anatomic prosthesis with patella resurfacing. The presence of patellofemoral pain correlates well with a poor AKKS, but the role of plain radiography and bone scintigraphy as investigative tools remains unclear.
The purpose of this study was to evaluate the reasons for patellar instability in modular rotating hinge TKR, with regards to design of the prosthesis offering unlimited rotation, component positioning and the role of compromised soft tissues.
We reviewed six patients with rotating hinge TKR operated over the past 3½ years for either ligamentous instability, bone loss or both. The problem of patellar instability was identified in all patients. Five patients had realignment of extensor mechanism for patellar maltracking, while the remaining one patient with patellar instability was asymptomatic.
Post-realignment the HSS scores revealed good results in 3 knees, fair in 2 and poor in 1 patient. All patients had a well aligned knee with satisfactory component positioning.
The unlimited rotation offered by the modular rotating hinge TKR because of the absence of a rotational stop causes excessive demands on the soft tissue and is a reason for patellar instability in patients with compromised medial soft tissue integrity.
The high incidence of patellar instability compromises the results of TKR and is a cause of concern and this implant should be reserved for patients with severe ligamentous instability and bone loss not amenable to ligament balancing.
Rapidly progressive cases of primary idiopathic hip osteoarthrosis are well known and recognised. The prevalence reported in the literature varies from 4–18%. Three types have been identified- type 1 (rapid), type 2 (moderate) and type 3 (delayed) depending on the duration of chondrolysis and the subsequent rate of bone loss per year.
We reviewed the charts of all patients deemed to be RPO type 1 who had underwent hip arthroplasty under the care of the senior author (DEB) over a two-year period in an attempt to identify risk factors, which may have contributed to the rapid progression of their disease. All patients were treated using a custom femoral stem and a spiked Duraloc cementless socket following careful preparation of the acetabulum.
We identified 34 patients (40 hips) with type 1 rapidly progressive osteoarthrosis. Over the same time period 991 patients had underwent primary total hip arthroplasty, giving a prevalence of 4%. Of the 34 patients, 29 were female of average age 70.6 years (range, 51–83 years). All of the bilateral cases (6 patients) were female. Body mass index (BMI) for the female group ranged from 20.6 to 41.1Kg/m2 (average, 28.2kg/m2) whilst that for the males was on average 25.8Kg/m2 (range, 23.4–29.7Kg/m2).
Preoperative erythrocyte sedimentation rate (ESR) was 18mm/hr on average for the female group (range, 2–65mm/hr) and ranged from 3–52mm/hr (average, 20mm/hr) for the male patients. The preoperative Oxford Hip Score averaged 51 points for the female group and 48 points for the male group.
A detailed review of occupational history did not reveal any common occupational hazard. The majority of patients were non-smokers and denied any regular alcohol intake. Twenty-two patients (65%) had a history of hypertension. Twenty-seven patients (79%) had a history of non-steroidal anti-inflammatory use (most common preparation-diclofenac). Twenty-four patients (71%) resided in a rural area.
When compared to a cohort of patients undergoing primary total hip arthroplasty over the same time period, the only statistically significant risk factor identified was female gender.
We conclude, that patients who develop rapidly progressive osteoarthrosis of the hip are difficult to identify due to the absence of specific clinical features. We also outline our experience in the management of these technically challenging cases.
Conventional banking of donated femoral heads has been well documented in the literature. It relies on screening potential donors, providing a storage facility and sterilisation techniques which are not standardised. Stored femoral heads have a finite lifetime and wastage does occur. Prion contamination and malignant potential are present with modern storage techniques.
We report a technique of banking the donor’s femoral head in a surgically fashioned subperiosteal pouch, under iliacus. Young patients requiring a total hip replacement who are likely to need revision at a later date are suitable candidates. Patients who have signs of loosening of their total hip replacement and contralateral osteoarthritis are also suitable. The femoral head is retrieved and used for the donor’s own revision surgery. Interim clinical results for 12 patients with the head harvested at a maximum of 5 years from implantation are presented. We report no morbidity at the pouch site and present radiographic results showing good integration of the morselised femoral head bone graft in revision hip surgery. Histological results are also presented.
Autobanking of the patient’s own femoral head has the advantage of providing a graft with a reduced risk of infection, rich in growth factors, with the potential of osteoinduction. It eliminates the need for a storage facility, screening programme and provides a portable storage facility if the patient moves area.
Aseptic loosening of the acetabular component is the main reason for revision hip arthroplasty surgery with loosening rates reported at 25% at 12–15years. The optimum method of acetabular preparation and cementation technique has not been fully evaluated. Clinical follow-up studies suggest multiple keyholes improve survival rates.
Keyholes increase penetration of cement and torsional resistance of the bone-cement interface. Some studies support the traditional three 1/2 inch keyholes other studies have shown multiple smaller holes improve stability. The optimum size and number of holes to provide the strongest fixation has yet to be determined.
Using an established 54mm diameter acetabular model, mahogany, three sizes of keyhole were tested-3x10mm holes, 12x5mm, and 48x2.5mm- the surface area of the defects created were the same in each group. The model acetabulum was filled with cement and a metal central bar inserted through which torque could be applied using an Instron machine. Six specimens from each group were tested. Three 10mm holes produced a significantly stronger resistance to torque when compared to 2.5mm (p≤0.017) and 5mm holes (p≤0.001). There was no significant difference between 2.5mm and 5mm holes (p≤0.139). Each addition of a further 10mm hole significantly increased the torque strength until the model was destroyed at six holes.
In laboratory testing larger key holes provide a stronger cement-acetabular interface.
The use of exhaust suit systems is commonplace in arthroplasty surgery where isolation of the surgical team is desirable in an attempt to reduce the risk of infection transmission. Elevated carbon dioxide levels have been reported in the non-clinical setting with such systems the consequences of which can include fatigue, diaphoresis, nausea, headache and irritability.
The aim of our study was to determine the levels of carbon dioxide present within an exhaust suit system during hip arthroplasty and to compare these with the recommended occupational exposure limit levels published by the Health and Safety Executive (HSE).
Data was collected during ten primary hip replacements performed by the same surgeon whilst wearing the Stryker Steri-Shield Helmet Exhaust System. This is a self-contained unit with an integrated blower used in conjunction with a full-length gown. In addition the helmet was fitted with an air-sampling probe connected to a portable infrared CO2 monitor and also a temperature probe. Thus continuous monitoring of both CO2 and temperature level during surgery was possible.
The mean initial CO2 concentration in the helmet at the beginning of surgery was 3000 parts per million (ppm) and the mean maximum CO2 level recorded was 13,000 ppm. The mean time the surgeon was within an exhaust suit to perform a primary hip replacement was 1 hr 54 mins and for 86% of this time period the CO2 level within the helmet exceeded the recommended level of 5000 ppm as stipulated by the HSE.
In conclusion we have demonstrated significantly elevated CO2 levels within the Stryker Steri-shield Exhaust Suit System during hip surgery. Surgeons who use this system should be aware of this together with the physical symptoms that may result.
A physiological hip simulator was used, loads and motions were applied to approximate
The aim of revision hip arthroplasty for infection is to eradicate infection and restore function. There is, in current literature, little evidence to suggest an optimal time interval between first (excision) and second (reconstruction) stage procedures in revision hip arthroplasty.
Our aim was to assess the difference in outcome, in terms of patient pain, function and satisfaction, in relation to the time interval between surgeries.
A prospective analysis was made of 22 consecutive patients who underwent two-stage revision total hip replacement between 1992 and 2001. There were 12 male and 10 female patients. The mean age at the time of revision surgery was 63.5 years (range 35–83 years). The indication for surgery was infection in all cases. Patients were subdivided into two groups according to the time interval between first and second stages : Group 1 – time interval 6 months or less; Group 2 – time interval greater than 1 year. Outcome was assessed at 1 year post-operatively using change in pain and function scores and patient satisfaction scores.
Pre-operative pain and function scores were similar in the two Groups. Both Groups reported a similar improvement in pain at 1 year post-operatively. The patients in Group 1 also showed an improvement in function score, however, the patients in Group 2 showed no improvement in function. All patients felt the operation to be worthwhile as reflected in the patient satisfaction scores.
The results suggest that good improvements in pain can be achieved after short and longer time intervals. A longer time interval may well be associated with a poorer outcome in terms of restoring function.
Blood transfusion is associated with an increased incidence of post-operative nosocomial infections following surgery. In a prospective study we evaluated the association of blood transfusion and the changes in the immune status with the incidence of infection in the post-operative period following primary hip arthroplasty and subsequently for two years following surgery
T-helper cell, cytotoxic T cell and NK cell activity was recorded using a Beckton Dickson flow cytometer and assays of Plasma viscosity, CRP, Staph. Epidermis and ASO titres were analysed. All infections were recorded for 2 years following surgery.
The incidence of nosocomial infections was reflected by a greater reduction in NK activity and CD4: CD8 ratio following surgery in patients receiving SAGM blood transfusion.
Homologus blood should be used judiciously in joint arthroplasty with a preference to either leukocyte depleted blood or predonated autologus blood.
Hydroxyapatite Ceramic Coated Hips (HAC) were first used in Sunderland, U.K. in May 1988. More than 1725 HAC hips have been inserted. There are 264 hips in 237 patients with ceramic/ceramic (alumina) bearings.
These hips are inserted into patients with a 20+ year life expectancy. Their mean age is 50.5 years.
All patients are assessed using the Harris Hip Score pre. and postoperatively. There are 14 patients with Harris Hip Scores of less than 80, but only 8 patients have problems attributable to HAC hip surgery. These include 1 patient with infection, 3 fractured ceramic acetabular liners, one broken ceramic head, 2 with aseptic loosening and 1 patient who chronically dislocated her hip.
Amongst the indications were osteoarthritis 136, hip dysplasia 44, and ankylosing spondylitis 13. Twenty six had had previous childhood hip disorders, and 16 had rheumatoid arthritis. The series also includes 4 revisions from cemented hip replacement.
The results have been rewarding. There are 1700+ HAC hips in the whole series. This sub group of 264 ceramic/ceramic HAC hips is small and follow up is relatively short. There have been few failures which could be attributed to the HA coated device. However, there are 4 broken ceramic components.
Wear in ceramic bearings will be negligible. Third body inclusions must be avoided.
The femoral spigot must not impinge on the acetabular margin. The ceramic material has to be supported to prevent fracture.
Currently, all details regarding implants are entered into a real time application on the Musgrave Park Hospital site using the Belfast Orthopaedic Information System (BOIS). This is a visual basic client application with data being stored in an SQL server database. This data collection system operates throughout every location within the hospital including the theatre block.
Loss of continuity occurs however when joint replacement takes place in Musgrave Park Hospital and then revision surgery or other procedures are carried out at other locations. The goal therefore of the Northern Ire-land Implant Register is to collect information on all implants performed and their revisions regardless of their location.
The dataset collected is based on the work of the National Joint Replacement Registry. Our system is designed to support and extend that dataset to provide a more comprehensive joint replacement registry database. This means that reports can be provided to individual sites and data entered into the National registry if required at a later stage.
At present every hospital in Northern Ireland is connected to the HPSS network (similar to the HPSSNet in the UK). What has been developed is a web browser based front end, which requires no complex software installation on any client machine. From this web based tool, staff at other locations can access information held at Musgrave Park Hospital, they can select an implant, or record a new implant and then link any revisions or other procedures carried out.
As all of the information is entered directly into the BOIS database, there is no delay in the information being available to all who access the system. This reduces the need for case notes to be transferred to other sites and the need to contact the other site directly regarding the case. The interface also provides a comprehensive reporting capability so that commonly requested standard reports are available for authorized staff to run from their web browser.
We present an overview of how the web interface works in practice and how data is entered into the system.
An audit of a group of dislocations (7 out of 66 hip replacements) revealed a problem with the Charnley Golf Ball cup when used with the posterior approach.
Sixty-six consecutive Charnley hip replacements in one institution by one surgeon using the posterior approach over a one year period are presented. The dislocation rate prior to the introduction of the Golf Ball cup was less than 1%. The overall dislocation rate after the introduction of the Golf Ball socket rose to 10.6%.
Four patients suffered one dislocation, 2 patients suffered two dislocations and 1 patient suffered a dislocation and spontaneous reduction. Five patients were revisions hip replacements and 61 primary hip replacements. Two of the revisions dislocated.
A study of the type of acetabular component type in this series showed there were 17 Wroblewski Angle Bore Sockets (WAB), 11 ogee long posterior wall sockets (OGLPW) and 38 golf ball (GB) sockets making a total of 66 hip replacements.
Of the 17 patients with the WAB the dislocation rate was 0 %. Of the 11 OGLPW patients the dislocation rate was 0 %. However in the 38 patients with golf ball sockets the dislocation rate was 18% (7/38). All the dislocations were anterior.
The acetabular component position was flexion 15–30 degrees (mode 30 degrees) and anteversion 0–10 degrees (mode 0 degrees). The numbers were not large enough to produce any statistical correlation. All femoral stems were set to 0 degrees anteversion.
Following this audit we discontinued the use of the golf ball socket with the posterior approach and have had no further dislocations in primary hip replacement using either the OGLPW or the WAB sockets.
Surgeons who use the posterior approach should be warned about the problems of a high anterior dislocation rate when using the Golf Ball cup.
Factors that allow the generation or ingression of wear particles at the implant-host interface after total hip arthroplasty (THA) may include early migration and periprosthetic bone loss. We have previously shown that a single 90mg dose of the bisphosphonate pamidronate prevents bone loss over 6 months after THA. In this 2 year randomised trial extension study we assessed the longer term effects of this intervention on bone loss and implant migration.
Twenty-two patients received 90mg of pamidronate and 22 received placebo at randomisation 5 days after surgery. Femoral and pelvic bone mineral density (BMD) was measured by dual energy x-ray absorptiometry (DXA) and implant migration was measured using the EBRA-Digital method over a 104 week period.
In the placebo group rapid periprosthetic bone loss occurred over the first 6 months. After this period a partial recovery in bone mass occurred in most regions. Patients in the pamidronate group had significantly less femoral, but not pelvic, bone loss than those give placebo (ANOVA P=0.02). Pamidronate was most effective in preventing bone loss in Gruen zones 6 and 7 (ANOVA P=0.004, and P=0.014, respectively). At week 104 the mean total stem migration was 1.77mm±0.27 and 1.62mm±0.37 for the placebo and pamidronate groups, respectively (P> 0.05). Total cup migration was 0.75mm±0.26 and 0.76mm±0.14, respectively (P> 0.05). Age at surgery accounted for 26% (linear regression r=−0.65, P=0.02) and 38% (r=−0.51, P=0.007) of the variability in stem and cup migration at week 104, with younger subjects experiencing greater migration. Stem migration at week 104 was also inversely related to the Barrack cement mantle grade (r=−0.66, r2 41%, P=0.0003). Implant migration was not significantly related to changes in periprosthetic bone mass.
Pamidronate therapy has a significant effect on bone mass, but not implant stability, after THA.Our findings suggest that the major determinants of early migration after THA are young patient age and poor cementing technique.
Revision hip Arthroplasty is a costly procedure, which is becoming more frequently indicated. We found that our unit revised a high proportion of hips that had been implanted in other health regions. A detailed cost analysis of a revision procedure was performed and has shown that the real cost is far more than the hospital finance department budget for. This represents a very significant cost to a trust for this type of surgery. The health care budget allocated to a trust does not take into account the geographic movement of the population. We estimate that the cost of revising hips, originally implanted in other regions, costs our hospital roughly the equivalent to a consultant surgeon’s salary per year.
During revision hip surgery, damage to the sciatic nerve is due most commonly to excessive tension. While the nerve is strong in tension and is able to tolerate this remarkably, it is sensitive to lateral compression against angled structures and it is likely that tension causes injury by such pressure.
In a personal series of 441 revision hip procedures, sciatic nerve injury occurred in 9 recognised cases:
2 were complete with no useful recovery
2 were severe with some incomplete recovery
3 were predominantly lateral popliteal with incomplete recovery
2 were transient and clinically fully recovered.
In only two of these were the cause and the time of injury identifiable. In these cases, pain was not a serious feature but in eight separate medico-legal cases, burning pain of variable distribution has been the most serious complaint. Medical negligence has been successfully sustained on the grounds of
We have found that in normal individuals the range of straight leg raising varies between 30 and 90 degrees. Towards the limit of this range the nerve is tight and a crude cadaveric test indicated a tension force of 40 newtons! In an athlete this may be extreme and yet the nerve does not complain. Excluding direct compression (e.g. by a retractor) and thermal injury, we suggest that the tension developed during unguarded straight leg raising while the patient is still anaesthetised is a serious risk factor. After even conservative lengthening, the tension rises alarmingly during such action. It is possible that pre-existing lumbar degenerative disk disease can contribute to the hazard and be source of pain.
There have been reports on the clinical survivorship of the Charnley Elite Plus (Depuy) hip prosthesis. We report the minimum five-year clinical and radiographic results of this implant in a consecutive series of one hundred and thirty-five primary cemented total hip replacements (THR) in one hundred and thirty-one patients. The mean age at operation was seventy-four years (range forty-one to ninety).
The operations were performed at a single centre by surgeons of different grades using the modular Charnley Elite Plus THR with CMW cement. The indications for surgery were osteoarthritis in 87% and rheumatoid arthritis in 13%.
The mean follow-up was five years four months (range five years to six years two months). At the most recent follow-up twenty-three patients had died and four patients were lost to follow up. Thirteen hips have been revised for femoral loosening. Eight of these were for aseptic loosening and five were infected. Ninety-five surviving hips were therefore available for review. Seventy were seen in clinic and twenty-five answered telephone questionnaires. Seventy sets of radiographs were available for assessment and of these a further three femoral components were radiographically loose.
Survivorship was calculated by constructing life tables using the end points of aseptic revision and definite radiographic loosening. Using this method the aseptic revision rate was found to be 7.26% at five years but if the radiological failures are included this becomes 10.15%.
Three different modes of failure were identified but there was no obvious single factor leading to what appears to be a high rate of aseptic failure.
The authors would suggest caution with selection of this implant until the clinical and radiological results of larger studies with a similar follow-up are reported.
Introduction: Long-term, aseptic loosening is the central problem for total hip replacements (THR)
Subsidence
0.20 ± 0.12 mm (15)
Internal Rotation
0.89 ± 0.52 deg (14)
Lateral
0.13 ± 0.09 mm (8)
External Rotation
0.16 deg (1)
Medial
0.11 ± 0.09 mm (7)
Valgus Rotation
0.09 ± 0.06 deg (5)
Posterior
0.17 ± 0.12 mm (11)
Varus Rotation
0.23 ± 0.14 deg (10)
Anterior
0.08 ± 0.08 mm (4)
Flexion
0.28 ± 0.15 deg (7)
Extension
0.15 ± 0.09 deg (8)
One hundred and ninety six unselected patients who had 200 consecutive primary total hip replacements between January 1994 and May 1995 using the Elite Plus cemented femoral component (DePuy International Leeds UK) were enrolled in a prospective outcome study. 155 patients (159 hips) were followed up for a minimum of 4.5 years (mean 5.4, range 4.5 to 6.9).Twenty four patients (24 hips −12%) died and 15 patients (15 hips) were lost to follow up. Two hips had been revised prior to the 5 year follow up. The average age was 68.4 years (range 35 to 94) at the time of the index arthroplasty. The patients were evaluated clinically using the Harris Hip Score and also radiologically. A self administered Oxford Hip Questionnaire was also used. A Kaplan-Meier survivorship analysis was performed with revision as the end point.
The mean Harris Hip Score was raised from 39.3 pre-operatively to 89.6 at five years. The mean Oxford Hip Score was 23. There were no revisions for aseptic loosening.
Radiographic review at 5 years showed mean femoral subsidence was 1.4mms with an average of 0.28mms per year. The cumulative survivorship at 5 years was 98.7% and the mean annual rate of re-operation was 0.2%.
In the present series, the Elite Plus hip arthroplasty has produced clinical and radiological results which would justify its position as a modern progression of the Charnley with comparable results at five years.
Fracture of the femur in association with total hip arthroplasty is a challenging complication that has been well described. A variety of surgical treatment options have been reported. We present our experience of the Kent hip prosthesis in the management of periprosthetic femoral fractures.
We reviewed all patients (46) who had a Kent hip inserted for a periprosthetic femoral fracture. This group consisted of 16 males and 30 females of average age 73 years (43–96 years) at the time of fracture. Follow up ranged from 2 to 85 months (average, 4 years).
In 26 cases the primary prosthesis was a Charnley stem. Of the remaining cases the primary prostheses were as follows: 6 Austin Moore prostheses, 5 Howse, 4 Custom, 1 Exeter, 1 DHS, 1 Richards and 1 Thompson stem. There were 6 intraoperative fractures. Of the postoperative fractures forty-four were associated with a traumatic event. Time to fracture varied from 3 weeks to 20 years (average, 8 years). Prior to fracture 42 patients were living in their own home and 24 patients were mobile unaided. Twenty patients had pain prior to their fracture. The majority of patients were deemed ASA grade II or III. Thirty fractures were Johanssen type II, 14 type I, and 2 type III.
At the time of surgery, 32 patients had a loose stem and/or cup. Operating time was on average 143 minutes (range, 65–235 minutes) and intraoperative transfusion requirements ranged from 0–7 units of packed red cells (average, 3 units). Duration of hospital stay was on average 23 days (range, 7–77 days). Two patients developed superficial wound infections, six patients dislocated their prosthesis and one patient developed a chronic wound sinus.
In 34 cases fracture union was complete at latest review. Three patients required revision surgery for stem breakage and in 10 cases there was evidence of screw breakage.
At latest review, of the 31 patients that could be contacted 18 are still resident in their own homes. Twenty-six patients require the use of a walking aid (most commonly one stick). Ten patients have ongoing pain in relation to their operated hip.
In conclusion, we feel that the Kent hip prosthesis is a useful surgical option in the one-stage management of periprosthetic femoral fractures.
Tumour necrosis factor-α (TNF) is thought to play a role in aseptic loosening, the major cause of implant failure after total hip arthroplasty (THA). Natural sequence variations at –238 and –308 in the promoter region of the TNF gene are associated with differences in the susceptibility and severity of several TNF-mediated diseases. We tested whether carriage of the [less common] ‘A’ allele at –238 and –308 are associated with aseptic loosening after THA.
481 Caucasians (214 with failed implants versus 267 with radiologically intact implants) were recruited 11.7± 4.1 years after cemented THA for osteoarthritis. Genomic DNA was extracted from peripheral blood and genotyped for the –238 and –308 polymorphisms using the Taqman® 5′ nuclease method. 500 subjects from the local population were also genotyped using Taqman® to establish the background prevalence of the ‘A’ allele at each site.
The carriage rate of –238A was 8.8% in the background population and 10.9% in the THA controls (P> 0.05). –238A carriage in the loosening group was 17.3% (odds ratio 1.72, 95% confidence interval 1.02 to 2.90). Carriage was highest (20.5%) in subjects with loosening of both the femoral and pelvic implant components (odds ratio 2.12; 1.17 to 3.83). The association of –238A with aseptic loosening was independent of age, sex, and amount of implant wear (Cox hazard ratio 1.49 (1.04 to 2.13; P=0.03)). Carriage of –308A was not associated with aseptic loosening.
Genetic, as well as environmental factors, influence implant failure after THA. Whether the –238 polymorphism causes the biological change that predisposes to loosening, or is in linkage disequilibrium with such a locus, is not yet known.
Proximal femoral fracture (PFF) is already epidemic and projected to increase. 50% of patients fail to recover their preaccident mobility, resulting in protracted hospitalisation and exposure to nosocomial (hospital acquired) infections which impairs recovery further.
The aim of this study was to establish the rate at which patients with PFF regain mobility, the point at which they cease to recover and the incidence, time of onset and effect of nosocomial infections.
Recovery of mobility and nosocomial infection was prospectively recorded in 170 consecutive patients with PFF. 53% regained their best level of mobility within 6 days of admission, 81% within 8 and 91% within 14. The mean hospital stay was 21 days and delay to discharge was 14 days. During the delay, mobility deteriorated in 22% of patients and 58% developed nosocomial infection of which 18 were methicillin resistant staphylococcus aureus. The risk of infection doubled after a delay of 6 days.
Protracted hospitalisation after PFF is unhelpful and dangerous to patients and wasteful of healthcare resource. There is a small window of opportunity to discharge patients after PFF that is often missed. Thus there are often no beds for patients with acute fractures because they are occupied by patients who do not benefit from hospital admission or remain because they have acquired iatrogenic disease.
Controversy exists with regard to the thickness of cement mantles that are necessary around the femoral components of cemented total hip arthroplasties. Conventional teaching, based on bench-top or computor models and theoretical analyses, as well as post-mortem & follow-up studies, suggests that the cement mantle should be complete and not less than 2–3mm in thickness. Mantles that are less than this are held to be at risk from mechanical failure in the long term; if they are incomplete, focal lysis may occur and progress to aseptic loosening.
However, long term experience with a number of French cemented femoral components suggests that these conventions may be erroneous. These French femoral components include the Charnley-Kerboull (stainless steel) and the Ceraver Osteal (Ti6Al4V) stems, in both of which the underlying design principle is that the stem should completely fill the femoral canal, the cement then being used purely to fill the gaps. Such a design philosophy implies that the cement mantles will be very thin, and since both of these stems are straight and the femoral medullary canal is not, the mantles may not only be thin, but also in places incomplete.
Conventional teaching would suggest that any stem utilising mantles of this type would fail from a combination of focal lysis and cement fracture. Yet the long term results of both of these stems have been outstandingly good, with extremely low levels of aseptic loosening and endosteal lysis, irrespective of the bearing combinations being used. Both these stems have a surface finish of Ra < 0.1 microns. A third French design, the Fare stem, manufactured from Ti6Al4V and based on the same principles, was associated with bad results when manufactured with a rough (> 1.5 microns) surface, and appreciably better results after the surface roughness was changed to < 0.1 microns.
These findings, that constitute the ‘French Paradox’, have profound implications for the mechanical behaviour of cement in the femur and for the mechanisms that underlie stem failure from loosening.
MRI is a well-tolerated, short procedure that would provide an early, accurate and cost effective diagnosis in elderly patients with negative plain films and persistent post-traumatic hip pain, thereby facilitating their correct management.
It is 100% sensitive and specific to occult hip fractures and does not involve ionising radiation.
Fractured necks of femur in the elderly population are common. This group of patients are responsible for a significant proportion of health care costs and efforts today. The diagnosis of hip fractures is not always clear-cut and plain radiographs may not show an undisplaced fracture. The management of this patient group is dependant upon the correct diagnosis via imaging and treatment decisions are based on these findings. If these fractures are missed, there is a significant chance of displacement and avascular necrosis presenting at a later date. This would complicate matters and result in more complex surgery. This also increases health care costs due to an extra admission, more expensive and difficult surgery with longer rehabilitation and after care. In our study, the management of the patients reviewed was significantly altered due to the imaging process used.
We performed MRI scans on thirty-six patients who had post-traumatic hip pain and negative plain radiographs (reported as normal or equivocal). Twenty-three (64%) of the patients sustained a fracture, of which sixteen (44%) involved the neck of the femur, all of whom were above the age of 71 years. 100% of the elderly age group scanned were positive for a femoral neck fracture and eleven (31%) received operative intervention. The five patients who did not undergo operative management were deemed too unwell for surgery. Only three patients’ scans were negative.
These results confirm that MRI (in the 71 years and above age group), is indicated in order to diagnose an undisplaced fractured neck of femur not recognised on plain radiographs, which requires operative intervention in the form of dynamic hip screw or cannulated hip screws to prevent further deterioration or displacement.
The bearing surfaces chosen were: metal / metal in 13%, metal on poly in 56%, ceramic on poly in 28% (Zirconia in 7.4%) and ceramic on ceramic in 3%. Low viscosity cement was used with 28% of femoral components and 19% of acetabular components. The predominant femoral head size was 28 mm.(49%) (22mm in 23%).
The generation of wear particles at the primary articulating interface of total hip arthroplasty is well documented. Particles may also be generated at the stem/cement interface in cemented prostheses. An investigation of explanted Capital femoral stems demonstrated that wear at the stem/cement interface had contributed to their early failure. This study compared the wear particle generated by stems of three different materials and with three different surface finishes. Three femoral stems were chosen as ‘templates’, one with a smooth surface,(the Exeter), one with a slightly roughened surface (the charnley) and one with a very rough surface (the capital). Their surfaces were measured and plates were manufactured with comparable surfaces in each of three materials in use for femoral stems, stainless steel, cobalt chrome and titanium alloy.
The plates were opposed to cement pins in a laboratory wear simulator. The volume of cement lost from the pins was measured and the debris generated was examined under the scanning electron microscope.
Analysis of the results demonstrated that for each of the materials tested, volume of wear particles generated increased as the roughness of the surface increased. When comparing similar surfaces in different materials it was also demonstrated that softer materials produced greater volumes of wear than harder materials.
The analysis of the debris demonstrated that material affected debris size; harder materials produced smaller cement particles than softer materials independent of surface finish.
Particles size and number of particles have been demonstrated to influence macrophage activity. The results of this study would suggest that softer materials should not be used for cemented stems with a rough surface finish.
This early study examines the influence of a wider shoulder on the 1 year migration of a cemented, polished, tapered stem, using RSA.
Polished, tapered stems (PTS) have excellent 10 year survival rates. RSA studies have demonstrated that these devices subside about 1 mm / year. Small amounts of subsidence are beneficial in stabilising a stem. Stem rotation (measured as posterior head migration) within the cement mantle is probably a more important mechanism of failure than subsidence. Stems with a wider proximal portion are thought to better resist rotation. The CPS (Endoplus, UK) is such a device; here we compare its’ stability with that of the Exeter.
20 patients received the CPS-plus stem and underwent RSA examinations at 3, 6 and 12 months postoperatively. The Exeter 1 year migration data was used as a comparison. Both groups underwent a Hardinge approach with CMW3G cement.
Both stems subsided about 1mm. The CPS showed less medio-lateral and A-P movement of the proximal stem than the Exeter over 1 year, as shown below:
The CPS internally rotates less than the Exeter, as demonstrated by the smaller amount of posterior head migration. It has a lateral flare of the shoulder; making its cross-section wider than the Exeter’s, this probably accounts for its’ greater resistance to rotation. The CPS also undergoes less medio-lateral proximal stem migration. Its’ lateral shoulder flare is probably responsible for this axial subsidence, as it prevents the shoulder from moving laterally whilst subsiding over the calcar.
A PTS with a broad proximal section is more stable, this may confer an increased survival advantage.
Bone cement with an antibiotic additive is currently widely available, gentamicin being the most common type. However, the high resistance of such organisms as staphylococci to gentamicin has popularised the practice of adding additional antibiotic powders to the cement mix.
This study aims to quantify the effects of adding 1g active of seven antibiotics on the viscoelastic properties of the cement from mixing to set time using a robust rheometer, developed at the University of Leeds. CMW1 Radiopaque cement was the base cement selected for its widespread familiarity.
Viscosity and elasticity were recorded at two rates of shear until the cements set. Viscosity was found to decrease with shear rate, but the cements were found to have a significant elastic component that greatly increased with shear rate. This indicates that for maximum cement penetration, maintained pressure would be more effective than “hammering”.
It should be noted that the effects described above are small compared to other theatre variables, especially temperature and humidity.
To maximise the long-term survivorship of any hip prosthesis it is important to recreate joint centre. Normal joint centre is determined by horizontal offset and vertical height of the acetabular and femoral components. In this study joint centre and horizontal offset were analysed in 200 consecutive patients operated on from October 1998 in whom the opposite hip was normal. Joint centre was defined relative to the acetabulum and femur both pre- and post-operatively. On the acetabular side a horizontal line was drawn across the pelvis immediately below each teardrop. A vertical line was drawn at right angles through the middle of each teardrop. Acetabular offset was defined as the horizontal distance from the vertical trans teardrop line to head centre. For femoral offset a screened x-ray was taken to show maximum offset. The anatomical axis was drawn and the offset was defined as the distance from the anatomical axis to head centre.
Our results show on the acetabular side there was an overall tendency to leave the joint centre medial and so decrease acetabular offset. However, we found that 90% of our sockets were placed within 6 mm of normal joint centre. We attribute this accuracy to the principle of visualising the transverse acetabular ligament intra-operatively and using this landmark to control depth of socket insertion. Conversely, on the femoral side there was a slight tendency to increase the offset. Nevertheless, 98% of the custom stems were within 10mm of normal joint centre. When we looked at total horizontal offset i.e. the combination of femoral and acetabular offset we found that joint centre had been restored to within 10mm in 93% of cases.
This study confirms the effectiveness of the custom femoral stem and Duraloc socket in restoring joint centre.
We followed up 83 patients who under went 92 Furlong Hydroxyapatite coated femoral stem, threaded acetabular component, and 28mm ceramic heads.
These hips were inserted between the periods 1989–1992 The Average age of the patients at the time of surgery was 54 years with an age range 31–67. And were followed up at 5,7,10 years respectively.
At the ten year follow up there were 64 patients with 70 hips. 5 hips were revised. 3 for acetabular component loosening, 2 for infection. 8 died from unrelated causes, 3 refused to attend but filled in the Oxford hip score by mail, 2 were lost to follow up. At the time of follow-up the average age was 64 years with an age range ( 41 – 77). The Oxford, and the Harris hip scores were used to Asses the patients clinically, and a standard AP pelvis X-Ray showing both hips was performed
Clinically we found. The average Harris hip score 90 ( 51 – 100), the average Oxford hip score 20 ( 12 – 45 ).
Radiographic assessment showed good component fixation with uniform bone growth around the components. The average angle of the Acetabular component was 52 ( 40– 60 ). 4 cups showed loose zones mainly in zone1. 21 hips showed polyethylene wear 6 had more than 2.5 mm wear. 52% of the hips showed proximal calcar remodelling, only 7 stems showed loose zones mainly in zone 1.
We conclude that the Furlong HA coated THR is an excellent THR for the young patient who has a higher activity demand with a survival rate of 93.9% excluding deaths and patients who refused to attend at ten years follow up.
The Use of bone allograft in orthopaedic Surgery has been predicted to increase particularly in joint revision surgery. This has led to a potential problem with supply. Questionnaires were distributed to all 146 Consultant orthopaedic Surgeons working in Scotland in 2000. They were asked to indicate their current usage of bone and tissue allograft, any problems encountered with supply and if alternatives to allograft such as processed bone, might be used. The questions asked were very similar to those asked in a survey by the author (GG) in 1995 to enable comparisons to be made. 74% of all bone issued by the SNBTS in 2000 –2001 was used in revision hip arthroplasy. This compares with only 66% of bone issued in 1998–1999.
Replies were received from 125 consultants (87%) of whom 93 reported using bone allograft. 41 consultants (46%) predicted an increase in their requirement for bone allograft, and 23 (26%) felt they could currently use more bone if this became available. Sixty percent of Surgeons would consider using processed bone as an alternative. In comparison with figures from a previous study in 1995, an increasing number of surgeons are prepared to use processed bone as an alternative to fresh frozen allograft. As the number of revision THR’ s continues to increase the amount of bone required is likely to continue to increase. The need to increase efficiency in harvest and supply of bone is therefore great. The use of more SNBTS nurses in selection of patients and collection of bone may increase efficiency. More surgeons may have to use processed bone, which would allow more bone to be released. Also processing may help reduce transmission of infective particles such as HIV and new variant CJD. With rising public and medical concerns over these issues this seems most desirable.
Twelve patients undergoing total hip replacements were given 600mg linezolid as a 20min intravenous infusion along with conventional prophylaxis of 1gm cefamandole immediately before surgery. Routine total hip arthroplasty was performed and at timed intervals during surgery, samples of bone, fat, muscle and blood were collected for assay by HPLC analysis. Samples of haematoma fluid that formed around the operation site and further blood samples were also collected at timed intervals following the operation for assay. The penetration of linezolid into bone was rapid with mean levels of 9.1mg/L (95% CI: 7.7–10.6mg/L) achieved at 10min after the infusion, decreasing to 6.3mg/L (95% CI: 3.9–8.6mg/L) at 30min. Correcting for the simultaneous blood concentrations gave values for bone penetration of 51% at 10min, 60% at 20min and 47% at 30min. although the penetration of linezolid into fat was also rapid, mean levels and degree of penetration were approximately 60% of those seen in bone at 10min: 4.5mg/L (95%CI:3–6.1mg/L; penetration 27%) 20min: 5.2mg/L (95% CI:4–6.4mg/L; penetration 37%) and 30min:4.1mg/L (95% CI:3.3–4.8mg/L; penetration 31%). For muscle, the corresponding values were 10min: 10.4mg/L (95%CI:8.1–12.7mg/L; penetration 58%), 20min 13.4mg/L (95%:10.2–16.5mg/L; penetration 94%) and 30min 12mg/L (95% CI:9.2–14.8mg/L; penetration 93%). Mean concentration of linezolid in the haematoma around the operation site were 8.2mg/L at 6–8h and 5.6mg/L at 8–10h after the infusion and 7mg/L at 2–4h following a second 600mg infusion given 12h postoperatively.
We conclude that linezolid exhibits rapid penetration in bone, fat and muscle of patients undergoing hip arthroplasty to achieve levels in excess of the MIC for sensitive organisms (MIC of < _ 4mg/L); with therapeutic levels maintained in the drainage which surrounds the operation site for more than 16h. This pharmaco-kinetic profile is similar to those of agents currently used for the treatment of bone and associated soft tissue infections and suggests a role for linezolid in the management of such patients
Obesity is increasing among patients requesting total hip replacement. Obesity is often considered though, a relative contraindication to arthroplasty surgery due to difficult access, greater blood loss, oozy wounds, poor mobilisation and delayed discharge. We have attempted to demonstrate the evidence for this.
Patients were evaluated preoperatively with regards to their height and weight to allow a body mass index (BMI) to be calculated. The length of inpatient stay was then monitored and early postoperative complications recorded. This data was used to assess if obesity or age could be used to predict a prolonged hospital stay caused by poor rehabilitation and early post operative complications.
The results of 70 consecutive patients between 1999–2001 are reported. The average age was 69.3 with a range of 46.5–85.4 years. The sex distribution was approximately 2:1 female to male (N=48:22 respectively). Two patients were identified as being under their recommended weight, 24 as healthy, 26 as over weight and 18 as obese. Urinary tract infection was confirmed by microbiological culture in 6 patients, superficial wound swab grew organisms in 5 patients while 2 developed culture positive chest infections. No thromboembolic events were recorded (Stroke, Deep Vein Thrombosis, Pulmonary Embolism) however one patient died of ischemic heart disease (BMI 35 obese). Data was examined by an Excel statistical package and an ANOVA plot produced.
No statistical relationship was found between obesity and infective postoperative problems. No delay in discharge was found when BMI was considered, R2 value of 0.0015,
F-significance 0.75. When age alone was considered R2 value of 0.003 and F-significance of 0.65 was recorded. When age and obesity were considered together R2 was 0.005 and
F-significance 0.57. We find no evidence of increased rates of early postoperative complications or delayed hospital discharge in obese patients with a BMI less than 40.
Recurrent dislocation of the hip is a difficult management problem. We have chosen to tackle this in a minimal way and avoid complex revisions. All patients were late dislocators, and the majority were older than 75 years with 4 patients being octogenarians.
A 7cm incision is made in the skin at the trochanter, the fascia is opened and the hip dislocated posteriorly the head of the hip is felt under the external rotators and they are opened in a minimal way. The cup is inspected for gross wear, no abnormality has been found. The PLAD is applied and fixed posteriorly after removal of minimal capsular and scar tissue, simple closure takes place with no drain.
This procedure has been performed on nine occasions in our unit and all cases remain successful at a mean followup of 18 months (2–35 months). Operation times varied between 28 –42 minutes (mean 36 mins). Blood loss is minimal. The patient can be mobilised right away and early discharge can be achieved. This technique seems an ideal management solution in and elderly population with a good cup and stem with recurrent dislocation for unknown cause.
Fifty five primary Ultima® hybrid all-metal (Johnson & Johnson Professional DePuy) total hip replacements (THR) were evaluated prospectively at a mean follow up of 24 months. Patients were selected according to age and activity levels. The mean age at surgery was 58 years (41–69 years). 33 males and 22 females were included in the study. Surgery was carried out for osteoarthritis in 52 patients and for non-union fractured neck of femur, ankylosing spondilitis and post slipped upper femoral epiphysis in the three remaining patients. A single surgeon (the senior author) through the posterior approach carried out surgery. All patients received the Ultima® porous coated titanium shell with a morse taper cobalt chrome liner and double wedge taper polished stem and modular head. Blood metal ion analysis was performed on a cohort of 24 patients using High Resolution Inductively Coupled Plasma Mass Spectrometry, sampling taken pre operatively and then repeated post operatively at 6 months, 1 year and then annually.
Clinical results reported at a mean follow-up interval of 2.016 years have been excellent, with no prosthesis to-date requiring revision and no component migration or radiolucuencies being identified on any follow-up radiographs. One patient has died and one is lost to follow-up. The following non-device related complications were reported in the group, 2 (4%) superficial wound infections, 1 (2%) dislocation, 1 (2%) thrombosis, 1 (2%) IT band defect and 2 (4%) impingement. The dislocation was treated with a closed reduction, the position of the component having been judged as satisfactory. The impingement has resolved by one year in both patients. The results of pre and postoperative blood metal ion analysis in a cohort of 24 patients demonstrate some elevated levels, these levels are similar to those previously reported in the literature.
The Ultima® hybrid all-metal THR may represent a valuable alternative in the younger, high demand patient.
12 patients requiring revision of a cemented Furlong total hip replacement had advanced corrosion of their titanium femoral stems. Thigh pain unlike that of loosening was a characteristic feature of presentation an average 38 months after implantation (range 20–58 months). Radiographs demonstrated fusiform periosteal thickening of the middle and distal thirds of the femur around the prosthetic stem with variable amounts of osteolysis around the tip. None of the femoral stems showed evidence of loosening and in 9 cases revision was solely for recurrent atypical pain.
The titanium stems were retrieved at an average 80 months (range 60–113). All were well-fixed but showed signs of advanced corrosion distally with blackened stems, loss of surface metal and thick white deposits. Two stems were examined with scanning electron microscopy and energy dispersive X-ray analysis. Micromotion abrasions were identified proximally with loss of all alloy constituents. Distally, there was selective loss of titanium in a pattern suggestive of crevice corrosion. This may be accelerated by a galvanic effect if a cobalt chromium head is mixed with a titanium stem.
After revision to an all stainless steel femoral stem and head, early follow-up demonstrates resolution of both symptoms and radiological abnormalities at an average 13 months (range 3–33) from revision.
Pyrexia in the post-operative setting has often been associated with a possible systemic or wound infection. We assessed whether there is any justification for our concern regarding post-operative pyrexia following hip arthroplasty and subsequent deep prosthetic infection.
An assessment of the clinical outcome of 97 sequential patients who underwent 103 primary hip arthroplasty for primary osteoarthritis replacements. Daily temperature and systemic complications in the post-operative period were recorded. Clinical outcome was measured using an Oxford hip questionnaire.
Patients had a mean follow-up of 5.2 years (range 3.5–7.2years).
A review of postoperative temperature records of 80 patients who had undergone primary total hip replacement. Thirty-one patients had required revision surgery at a mean time interval of 37.2 months (range 5–74 months) for confirmed deep prosthetic infection. The remaining Forty-nine patients were asymptomatic at a mean follow-up of 31.5 months.
Post-operative pyrexia of 38 degrees Celsius was present in 51% of patient’s undergoing primary hip replacement in the first post-operative week but in 21.1% no etiological cause could be identified. Clinical outcome measured by an oxford hip questionnaire was not influenced by the post-operative temperature pattern.
The mean peak temperature on the first post-operative day was significantly lower in patients with deep prosthetic infection then patients with a clinically normal outcome (p=0.01).
Discussion: This study has shown a high dislocation rate for a COP bearing that was reduced to a low dislocation rate by changing the bearing surface to a MOM design. A potential mechanism for this may be the ‘suction fit’ from the surface tension of the low clearance, high tolerance that the metal-on-metal bearing possesses, requiring increased torque to dislocate during impingement.
This study was performed to evaluate the pre-operative concerns of patients undergoing total knee or hip replacement surgery.
A cross-sectional study of 370 patients was performed. The patients completed a postal questionnaire on 29 concerns, each rated on a scale of 1 (not concerned) to 4 (very concerned). SF-12 and Oxford knee or hip scores were also calculated. Analysis was carried out using chi-squared tests on SPSS.
217 questionnaires were returned. The results showed that the greatest concern for patients was cancellation of their operation. This was followed by failure of the operation to reduce pain, loss of a limb and joint infection. Concerns regarding scar problems, nursing care and preoperative tests were the lowest.
Women showed statistically significant greater concerns in 9 areas. Younger patients (age< 65) showed increased concerns in 8 areas. Patients who had previously undergone joint replacement were less concerned than those who had not had previous lower limb joint replacements for 6 responses. They showed increased concern in 2 areas, nursing care and hospital food. Those undergoing total hip replacement were more concerned about dislocation, dressing and returning to work (all p< 0.05). The mean Oxford Knee or Hip Score was 42.96 and 45.12 respectively (scale 12–60, 60 being most severe symptoms). The mean SF-12 scores were 41.14 for the mental component and 28.70 for the physical component score (scale 0–100, 100 representing greatest level of good health).
The mean level of concern is low at 1.9 (scale 1 to 4). It is encouraging that patients who have had a previous joint replacement are generally less concerned. Possible reasons for increased concerns amongst women and younger patients are discussed. SF-12 and Oxford Knee/Hip Scores are comparable with other studies.
In conclusion, this study provides useful information for the preoperative counselling of patients, production of preoperative literature and for improving the service we offer to our patients.
This study describes percutaneous method of tennis elbow release and medium term results.
This novel modification of the posterior approach allows a low hazard exposure and easier surgery to the radial head.
Placed under cyclic strain at a physiological magnitude for 10 minutes at 1Hz using well established controls. Samples of media were analyzed for changes in NO and the cells were reacted for ALP activity, or: Stimulated with dexamethasone, (an established mediator of osteoblast differentiation) then reacted for ALP activity.
The long term results of the ulnohumeral arthroplasty have not previously been reported using a recognised elbow scoring system.
Kashiwagi reported his results in 1986 but no validated scoring system was used in the publication. Morrey in 1992 evaluated his results using the Mayo Elbow Performance Score but the mean follow-up interval was only 33 months.
Between 1990 and 1996 twenty consecutive ulnohumeral arthroplasties were performed for primary degenerative disease of the elbow.
Outcome assessment using the DASH questionnaire and the Mayo Elbow Performance Score was taken at a mean follow-up of 75 months (range 58 to 132). Excellent or good results were identified in 85% (17/20) using the DASH questionnaire, and 65% (13/20) on assessment with the Mayo Elbow Performance Score (correlation coefficient 0.79).
Eighty percent (16/20) felt that the benefits of surgery had been maintained, and of those working at the time of surgery, 75% (12/16) were still employed in the same vocation.
There was no correlation between radiographic recurrence and the degree of fixed flexion deformity, flexion arc or elbow scores.
Between 1993 and 2002 7 allografts/joint replacement combinations have been used to treat massive bone loss at the elbow.
The original 4 procedures (2 humeral and 2 ulna allografts) used a standard Stanmore total elbow replacement. Of these the 2 humeral allografts failed and revision surgery was necessary. The 2 grafts on the ulna side of the joint remain in situ (average 6 years after surgery) with one of the patients subsequently having a primary joint replacement on the contra-lateral side.
More recently a further humeral and a further ulna allograft/joint replacement have been performed together with one patient having humeral and ulna allografts on both sides of the joint for extensive bone loss. In these cases the Coonrad-Morrey total elbow arthroplasty was used as the joint implant.
The philosophy behind the use of allografts is discussed and the management principles outlined. The possible reasons for failure of the early humerus allograft/joint replacement combinations is addressed and future developments considered.
Steroids are known to have an adverse effect on the blood glucose levels in diabetics. Intra-articular steroids are commonly used in Orthopaedic and Rheumatology practice. However we have failed to identify any studies to date that have been carried out on the short-term effect of intra-articular steroids in diabetics who are taking insulin. This study was carried out to establish the effects of intra-articular (IA) steroid injections on the blood glucose levels and insulin requirements for insulin dependant diabetic patients treated for a “Frozen Shoulder”.
Surgeons can use ultrasound with confidence, the Sonosite scanner is accurate at detecting full thickness tears, calcifications may be over-reported. LHB can be assessed beyond the reach of arthroscopy and 191 patients have avoided an 8 month wait for a ten minute procedure. However the surgeon was placed under extreme duress by the radiology department attempting to block him from improving his service.
5A large amount has been written about whiplash injuries of the neck, but many of these patients are often referred to shoulder units for assessment either acutely or years after the accident because of continuing symptoms. Although neck pain is the commonest complaint tenderness on examination is sided and within the trapezius muscle in virtually all cases. Pain referred to the shoulder is also reported in 36 – 67% whilst interscapular pain occurs in 20 – 72%, depending on the time from injury.
We have reviewed a personal series of the senior author of over 700 cases. The consistent finding in these patients is tenderness localised to a specific part of the trapezius in the base of the neck, which is sided. Tenderness on the same side is also present along the vertebral border of the scapula to its lower pole in over 90%, provided the scapula is protracted. A further finding in some patients is a high arc of pain on abducting the arm, thus simulating an acromioclavicular joint problem, but in these cases the pain is localised to the trapezius. These findings are in addition to those of the neck, which may show some restricted movement due to pain.
The trapezius tenderness can be abolished by the injection of local anaesthetic into the trigger spot at the base of the neck (whiplash injection test), which also resolves most of the above signs and allows further assessment of the shoulder without the referred pain from the injected area.
In vivo loading data for the rotator cuff would be of value to scientists and clinicians interested in the shoulder in the testing of surgical repairs, design of rehabilitation programs and for finite element models.
A technique for insertion and retrieval of the Arthroscopically Insertable Force Probe (AIFP - Microstrain Inc. Burlington, Vermont, USA) from the subscapularis is described was initially established in a cadaveric model. Ethical approval was obtained for AIFP insertion into the subscapularis tendon of volunteers during diagnostic shoulder arthroscopy. An in situ calibration was carried out using a modified arthroscopic grasper ( Smith and Nephew, Huntingdon, UK). After motor effects of interscalene block had worn off dynamic data relating to subscapularis tendon loading was collected. The AIFPs were removed through a port site by traction on an O (3.5 metric) nylon suture without complication.
Maximum loading of the subscapularis tendon was measured during internal rotation from neutral with the arm fully adducted. Forces measured exceeded 200N.
This paper describes a novel technique for the insertion, calibration and retrieval of AIFPs from the rotator cuff. In vivo tendon loading data was obtained. The techniques described may be applied to other structures of interest to orthopaedic surgeons.
Surgeons often protect Tendon-bone reconstructions such as rotator cuff repairs by off loading them. We investigated the effect of limb position and boundary conditions in an in-vitro rabbit patella tendon-bone repair model. Patella tendons were repaired back to the tibia in eight hindlimb cadavers with 2 mitek anchors(Mitek, Westwood, MA) and 3-0 Ethibond (Ethicon, Sommerville, NJ) using two techniques, one involving simple sutures and the other involving crossing over between the sutures. A loading mechanism through the patella tendon was constructed using static weights over a pulley mechanism. The contact area and force at the PT-bone interface were measured using a TekScan pressure sensor (6911, TekScan, South Boston, MA). The contact footprint (area and normal force) was acquired under four configurations: (1) knee full extension with interface unloaded, (2) knee 45° flexion with interface unloaded, (3) knee full flexion with interface loaded by limb weight alone, (4) tendon loaded with limb weight and 20N force applied through tendon loading mechanism. The contact area force footprint changed substantially between the different suture techniques and loading configurations. Crossing over of sutures appears to provide an increased and more evenly distributed force across the tendon-bone interface. Repair off-loading was accompanied by a decrease in the contact footprint force and pressure. The force in both suture techniques increased with increasing flexion angle and was substantially increased by both bearing the weight of the dependent limb and by an axial load in the patellar tendon. Off loading a repair may not provide optimal environment for healing.
Rheumatoid arthritis results in pain and loss of function due to gradual destruction of articular cartilage. The shoulder joint is frequently involved and a prosthetic replacement of the humeral head can restore function and relieve pain. Deficiency of the rotator cuff is common in patients with rheumatoid arthritis. Longevity of movement at the intraprosthetic interface of the bipolar shoulder prosthesis is debatable and has not previously been studied in rheumatoid arthritis.
We report a radiological study of the intraprosthetic movements of a bipolar shoulder replacement in 25 shoulders in 20 patients with rheumatoid arthritis of mean age 66 years (SD 10 years). Shoulders were X-rayed at a minimum of 3 and a maximum of 10 years from surgery. Measurements were repeated in 12 shoulders 3 years later. The patient was positioned in the scapular plane. An initial X-ray was taken with the arm in neutral and a further X-ray taken with the arm in full active abduction. Measurements were taken to determine the movement at the intraprosthetic interface and at the prosthesis/glenoid interface. Interobserver error and intraobserver error were determined using an intraclass correlation coefficient (ICC). A paired T-test and Pearson Correlation Coefficient were used to compare intraprosthetic movement with prosthesis/glenoid movement.
We found that intraprosthetic movement was preserved up to 10 years from surgery. However, there was no significant difference between intraprosthetic movement and shell/glenoid movement, with some shoulders exhibiting paradoxical movement at the intraprosthetic interface. Repeating the measurements after a 3 year interval in a subgroup of 12 shoulders showed a significant difference in intraprosthetic movement. Interobserver and intraobserver reliability for measurements of the movement at the intraprosthetic interface were excellent with a
We conclude that movement of the bipolar shoulder prosthesis in rheumatoid shoulders at the intraprosthetic interface is preserved up to 10 years from operation but is not related to or significantly different from prosthesis/glenoid movement and requires further investigation.
The purpose of this study was to look at the results of using the Copeland surface replacement in the treatment of arthritis of the shoulder.
We report the results of 61 Type 3 Copeland surface replacements in 57 patients. Operations were performed in 33 cases of Rheumatoid Arthritis, 27 cases of Osteoarthritis and 1 case of posttraumatic arthritis. Hemiar-throplasty was performed via a Deltopectoral approach by the senior author in all cases. There were 38 females and 19 males with a minimum follow up of 1 year and a mean follow up of 26 months (range 12–65). Patients were scored pre and post operatively using the Constant score. Average pre-op score was 15.6 and post-operatively was 52.5. There was one case of loosening ( ? secondary to infection) requiring revision to a stemmed implant. Two patients required Sub-Acromial decompression for postoperative impingement. All patients considered their shoulder improved following this procedure. There was no evidence of radiolucency in any postoperative radiograph.
Cementless surface replacement arthroplasty in our series show similar results to previously reported series of stemmed implants and to the published results available for this implant.
From 1998–2000 inclusive, we treated 155 acute, non-pathological fractures of the clavicle in adults. We reviewed 134, of which 95 were involving the middle third. The average time of follow-up was 24 months (range 9–33). Aim of this retrospective study was to review the results of operative versus conservative treatment in a view to create a standard protocol for these fractures management. Men accounted 67 the average age being 26.8 (range 15–83) and 28 were women with average age 36.8 (range 23–91). We operated on 23 patients: 3 due to neurological symptoms of C6 nerve root irritation, 4 due to a symptomatic non-union, 10 due to severe displacement and comminution with pressure on the overlying skin and 6 due to their request in a view to earlier return to activity as they were skilled athletes. All fractures healed within 6–14 weeks, and return to normal activity level was 8 weeks on average ( range 2–12). A 3.5mm DCP plate was used in all cases. We treated conservatively 76 patients. Non-union was encountered in 4 (4.2%) and was symptomatic in all of them so they were fixed with a 3.5mm DCP plate and bone grafted. The healing rate was 8–20 weeks, and return to pre injury activity level was 16 weeks on average (14–24). Unsatisfactory results reported from 23 patients, 21 of who were treated conservatively (27.6%) and only 2 operatively (8.7%). In the group of patients treated conservatively initial shortening was similar to the final and when 14mm or more was strongly associated with poor results. In the group treated operatively no significant shortening was found. We recommend young, active patients should be given the option of operative treatment in a view to earlier return to activities with a possible better clinical outcome.
Evaluation: In this retrospective study, the patients’ shoulder function, rate of fracture union, and complications between the three different types of plate were evaluated and compared.
The average follow up period was 6 years (range 4.5 – 9 years). The Oxford Shoulder Score revealed that 72% had good to excellent results, 16% remained unchanged and 12% were worse than prior to surgery. The corresponding DASH scores were 28% excellent, 40% good, 16% fair and 16% poor respectively. In addition 81% of patients were independent with daily activities, with 48% of them living alone and the remaining 33% living with their partners. Only 19% of patients needed significant help with their activities of daily living. These results were irrespective of whether surgery was performed on the dominant or non-dominant shoulder.
The Halder Nail was introduced into the UK in 1994 and the inventor has recently reported his results (Halder et al, 2001
The purpose of this study was to determine arthroscopically the pathology following anterior shoulder dislocation and assess visually whether rotation of the arm affected the reduction of the capsulolabral complex in cases where this was detached.
Over a sixteen month period from December 2000 to March 2002 we have arthroscoped and followed up prospectively a cohort of thirty patients. All patients were immobilised in a sling for four weeks and rehabilitated in a similar fashion with physiotherapy. The average age of the patients was 31 years and all patients were arthroscoped within six weeks of injury. The Hill Sachs lesion and capsulolabral complex injury were the most common pathology and were seen in two thirds of the patients. In the remaining group capsular tears and stretching were the most frequent injuries seen.
Injuries to the capsulolabral complex were seen in 22 patients. In seventeen of these the capsulolabral complex was still mobile and the time to arthroscopy averaged 10.3 days (Range 0–25). In the remaining five patients the labrum had healed in a malreduced position. The average time to arthroscopy in these patients was 30.8 days (Range 19–42).
In the patients where the capsulolabral complex had not reattached 14/17 (82%) patients demonstrated a better reduction of the labrum onto the glenoid with the arm in external rotation.
Based on these findings we conclude that:
The traditional use of a sling with the arm internally rotated may contribute to the capsulolabral complex healing in a malreduced position. This may be a contributory factor to the high redislocation rates found in young adults. Splinting the arm in a position of external rotation for four weeks may allow better reduction of the capsulolabral complex onto the glenoid.
Outcome was not related to the direction of instability, type of radiofrequency probe, age or ligamentous laxity. Two patients had a transient reduction in sensation in the axillary nerve distribution. 22 of 38 (57.9%) patients returned to their pre-instability level of sporting activity.
Arthroscopic stabilisation of the shoulder is a technically-demanding and developing technique, and the reported results have yet to match those for open surgery. We present a consecutive initial series of 55 patients with post-traumatic recurrent anteroinferior instability managed since September 1999 using a titanium knotless suture anchor. Patients were reviewed from 12–33 months postoperatively and assessed using the Rowe, Walch-Duplay and Constant scores. Following mobilisation of the capsulolabral complex, labral reconstruction was achieved using a two-portal technique and an average of three anchors placed on the glenoid articular rim. In 13 cases, additional electrothermal shrinkage was required to reduce capsular redundancy in the anterior and inferior recesses following labral repair, although 11 of these were in the first 18 months. Incorporation of a south-to-north capsular shift has reduced the need for supplementary shrinkage. Complications have included one instance of anchor migration requiring open retrieval and two documented episodes of recurrent instability, although these occurred in patients having surgery within the first six months after the introduction of this technique. Based on our initial experience, we believe that arthroscopic labral repair is a viable alternative to open Bankart repair and have now expanded the indications to include patients with primary dislocation, those participating in gymnastic and contact/collision sports, and revision cases with failed open repairs.
The effectiveness of steroid injection in the treatment of primary osteoarthritis of the acromioclavicular joint (ACJ) has been questioned.
We prospectively evaluated the outcome of 20 consecutive patients (25 shoulders) with clinical and radiological evidence of primary ACJ arthritis after steroid injections. All patients were evaluated using the Constant score after a minimum of 12 months follow up. Only patients with a negative provocative test after injection of 2ml of depomedrone and lignocaine were included in the study.
Eleven females (14 shoulders) and 9 males (11 shoulders) were included. The average age was 53.9 years. The mean preinjection score was 61.6 points (SD 13.12) and at 6 months this improved to 81 points, mean difference of 19.36 (CI = 14.19 – 24.53), p< 0.01, which was highly statistically significant. There was further improvement at 12 months, on the 6 month score, mean 88.4 points, mean difference of 7.4 (CI = 3.55 – 11.25), p = 0.001 which was also statistically significant.
In addition, the younger the patient, the greater the improvement in the objective score which measures the range of movement and power (r = −0.47; p = 0.01).
We conclude that local steroid injection is an effective method of treatment for primary isolated acromioclavicular arthritis and improvement continues for at least 12 months, but may require more than one injection.
All tests were repeated at the minimum of 6 (average 6.3) months after the operation.
CLINICAL
- 23 (95.83%) improved subjectively, and were back to their normal daily routines. - The average improvement in VAS scoring was an average of 3.5 (2–7)) - Impingement signs disappeared in 23 patients (95.83%) - Average increase in Constant score was 23 points, from 53.5 to 76.5.Average pain increased from 7.5 to 9, ADL from 5.5 to 6, hand position from 7 to 8, range of motion from 21.5 to 37 &
power from 9 to 17. Dynamometer Muscle testing (All measurement of power was done in watts)
A-Abduction power increased from an average of 14.5 to 32.9, Adduction from 17 to 42 b- At maximal adduction internal rotators increased from 25.5 to 34.55, external rotators from 20.25 to 30.85 and c- At 90° abduction the internal rotators increased from 19.55 to 31.3, and the external rotators from 16.6 to 21.95
-ASD provides good pain relief -Most patients return to work before the end of 6 months period; however there seems to be a tendency for further improvement after the 6 months period. - Muscle power increases post-operative but with individual variation -Dynamic Power assessment is preferable to the Constant Score method, as power is measured in Watts, and can test below 90° of elevation. -Power measurement is the only parameter directly related to the clinical outcome of ASD.
Where a plica was present the impingement lesion seen on the cuff side was significantly greater than the lesion seen on the acromial side (p< 0.0001). This suggests that the impingement might be due to the plica itself.
Recently concerns have been raised as to the effect of intra-articular radio-frequency energy on axillary nerve function. In our unit 120 shrinkage procedures have been performed with 5 intra-operative contractions of deltoid and no axillary nerve palsy. In this study we aimed to identify and quantify any changes in axillary nerve function following capsular shrinkage. Needle electrodes were inserted into the deltoid muscle of 10 patients undergoing radio-frequency capsular shrinkage and 3 patients having diagnostic arthroscopy. Recordings of Compound Muscle Action Potentials (CMAPs) were made following pre-operative magnetic coil stimulation of the axillary nerve. The nerve was then monitored during operation. At the end of the procedure, a further recording of CMAP following axillary nerve stimulation was made to allow comparison with initial readings.
We have shown:
Low amplitude stimulations of the axillary nerve in 6 of the 10 patients undergoing shrinkage. Increase in latency of the axillary nerve was noted in some patients including the controls. Increase in latency was independent of time spent performing shrinkage.
We have concluded:-
Stimulation of the axillary nerve occurs frequently during capsular shrinkage. This axillary nerve stimulation cannot be causally related to the application of radio-frequency energy. Increased latency may occur due to cooling of the nerve by extravasated irrigation fluid. Nerve monitoring is recommended during the training of surgeons new to this technique.
We would like to acknowledge the Magstim Company for their assistance with this project.
Dislocation after primary total hip arthroplasty (THA) is a devastating and frequent postoperative complication. Many risk factors for dislocation have been identified, however, thus far there has been no consensus whether inflammatory arthritis is a risk factor for dislocation or not. We carried out a prospective study assessing the prevalence of dislocation within 2 years after primary total hip arthroplasty for osteoarthrosis and inflammatory arthritis.
Between 1996 and 1999 312 patients (342 hips) with either a primary or a posttraumatic osteoarthrosis (OA group) and 59 patients (69 hips) with rheumatoid arthritis or other forms of inflammatory arthritis (IA group) were operated. One single type of prosthesis was implanted (EPF-PLUS® cup and SL-PLUS® stem) using an anterior approach. All dislocations in the two years following surgery were recorded. Both diagnostic groups were compared for known risk factors such as old age, female gender, prior hip surgery, and experience of the surgeon. Radiographs were examined for avulsion fractures of the tip of the trochanter and signs of loosening. The abduction and anteversion angles of the acetabular component were measured. Statistical analysis was performed with the Chi-square test and Student’s t-test.
The dislocation rate for inflammatory arthritis patients was significantly greater than that in patients with osteoarthrosis: 10. 1% (7 hips) in the IA group, 2. 9% (10 hips) in the OA group (p = 0. 006). There were no other differences in risk factors favouring dislocation in the IA group, such as old age, female gender, prior hip surgery, experience of the surgeon, trochanteric fractures or malposition of the prosthetic components. All dislocations in the IA group were posterior and occurred without any kind of trauma. In contrast, nearly half of the dislocations in the OA group were anterior and two were of traumatic origin.
Taking into account the fact that there are no differences in known risk factors for dislocation between our two groups and no differences in complication rate, except for dislocation, we can say that inflammatory arthritis has to be considered an independent risk-factor for dislocation after primary total hip arthroplasty. It may be that inferior quality of the (pseudo) capsule and the muscles stabilising the hip joint due to inflammatory arthritis leads to inadequate soft tissue tension. Another factor can be the concomitant impairments in rheumatoid patients, such as impairments of the upper extremity, ipsilateral knee or contralateral hip, leading to hyperflexion in the operated hip causing a posterior dislocation without trauma.
The concept of a new developed cup arthroplasty (Durom-Cup) is the replacement of the destroyed joint surface with minimal bone resection. In cases of additional cuff arthropathy the cup can be placed in a more valgic position to articulate with the glenoid and the acromion. The aim of this prospective study was to evaluate the results of this surface replacement as a hemiarthroplasty in rheumatoid arthritis with and without cuff arthropathy.
35 Durom-Cups of 29 patients (23 woman, 6 men) with rheumatoid arthritis were evaluated preoperatively and every 3 months postoperatively. 7 of these shoulders additionally had cuff arthropathy. The average age was 61. 6 ± 11. 8 years and the average follow-up 33. 4 ± 11. 8 months. The Constant-Score and SAS-function-Score were used and the cups were examined radiologically.
In rheumatic shoulders without cuff arthropathy the Constant-Score increased from 20. 6 ± 9. 5 points preoperatively to 47. 1 ± 14. 8 points 3 months postoperatively, to 47. 4 ± 13. 7 points 6 months, and to 56. 3 ± 8. 8 points 9 months postoperatively. During further follow-up it increased slightly and was 59. 5 ± 10. 1 points 12 months, 61. 8 ± 11. 3 points 18 months and 64. 6 ± 14. 8 points 24 months postoperatively. In shoulders with cuff arthropathy the Constant-Score increased from 17. 6 ± 8. 2 points preoperatively to 45. 0 ± 6. 4 points 3 months postoperatively, to 45. 5 ± 8. 5 points 6 months, and to 51. 5 ± 838 points 9 months postoperatively. At this level the Constant-Score stayed during further follow-up and was 54. 1 ± 10. 5 points 12 months, 56. 3 ± 9. 8 points 18 months, and 56. 1 ± 11. 6 points 24 months postoperatively. No complication, component loosening, or changes of cup position were observed.
The results of the Durom-Cup are encouraging. In shoulders with additional cuff arthropathy the limited goal criteria were reached always. Therefore cup arthroplasty is a good alternative other kinds of shoulder endoprostheses in rheumatic shoulders with and without cuff arthropathy.
The thrust plate prosthesis is an implantat with metaphyseal fixation at the proximal femur, which leaves the diaphyseal bone untouched. Therefore this implant preferably is employed in younger patients. It is dependent on a good bone quality in the proximal femur. Because bone quality is reduced in patients with polyarthritis, this kind of endoprosthesis may have a higher failer rate than conventional stemmed endoprostheses in these patients. Therefore in patients with polyarthritis even short- end midterm results of the thrust plate prosthesis should be analyzed.
47 thrust plate prostheses were implanted in 42 patients with polyarthritis (29 with rheumatoid arthritis, 6 with juvenile chronic arthritis and 7 patients with spondarthritis) and followed prospectively. The average age at the operation was 40. 8 ± 10. 7 years. Each patient was clinically and radiologically examined preoperative, 3 and 6 months after the operation and at the end of each postoperative year. The mean follow-up was 26. 1 ± 10. 7 months. The clinical findings were evaluated using the Harris-Hip-Score. Radiologically 8 different zones at the thrust plate prosthesis were analyzed for radiolucencies.
During the first year the Harris-Hip-Score rose continuously from the preoperative average of 42. 4 ± 6. 5 points to 78. 8 ± 10. 3 points 3 months postoperatively, 82. 3 ± 9. 8 points 6 months postoperatively, and 86. 8 ± 10. 1 points 1 year after the operation. The following examinations showed Harris-Hip-Scores at the same level. 5 patients (5 joints, 10. 6%) had to undergo a revision of the thrust plate prosthesis due to aseptic loosening in 3 cases and septic loosening in 2 cases. 6 prostheses (12. 6 %) showed radiolucencies, mostly below the thrust plate in zone 1 and 2. 2 of these prostheses were certainly radiologically loose which raised the failure rate to 7 of 47 (14. 8 %).
The thrust plate prosthesis improves function and pain in patients with polyarthritis to a satisfactory degree. Concerning the failure rate this type seems to yield slightly worse results than cementless stemmed endoprostheses in the same patient group. Due to the preservation of the diaphysial bone of the femur and the possibility of an unproblematic change to a stemmed endoprosthesis the thrust plate prosthesis keeps its indication in younger patients with polyarthritis.
One hundred fifty one total hip arthroplasty (THA) with metal on metal hip system of without cement were followed at a mean of 5. 5 years (range 2. 6 years to 7 years). Original diseases were 134 hip in 123 cases with osteoarthritis and 17 hips in 13 with rheumatoid arthritis. The average Harris hip score of before the operation was 45. 3 points and at the follow-up time the average score was 88. 5 points.
Radiographic findings in the incidence of partial radiolucent line around the component: in the acetabular component, no radiolucent line was observed, in the femoral component, marginal lucent lines were 8. 6% (13 hips). Cortical hypertrophy was observed in high ratio of 27. 2%(41 hips). There was no loosening and tilt of component over 5 degrees observed in any patient. Postoperative dislocation of the hip was observed 9 hips (6. 0%).
Cobalt concentrations and chromium concentration in the serum were measured in cases in metal on metal total hip, metal on poly arthroplasty and in controls without implants. Serum was assayed using graphite furnaces atomic absorption spectrophotometer. No patients were seen of elevation in serum cobalt and chromium concentrations.
The authors conclude that THA with metal on metal system has presented excellent results for mid term follow-up in our hospital.
Although silicone finger implant has several disadvantages including loss of motion, implant breakage and osteolysis, Swanson or other silicone prosthesis are still most widely accepted in the world. Osseointegrated implant showed great improvement as for as stem fixation, however, still used silicone joint with high incidence of fracture. Cement-less surface type finger joint prosthesis has been developed and clinical trial has carried out. Ninety three joint replacement in 30 hands with mean follow up about 2 years are reported.
The endoprosthesis consists of 3 different parts; two titanium joint anchor (fixture) in proximal and distal, titanium joint head in proximal, and HMWDP joint socket in distal. The joint anchor has tapered self tapping screw in joint side surface and has two flat long legs attached toward canal side which spread and compressed to intramedural canal firmly by turning a locking screw within the joint anchor. Each joint component is fixed to the anchor within a square hole. The MP joint component has anatomical head but semiconstrained toward volar dislocation by deep dorsal roof shape of the joint socket. Each socket has 2 different thickness. Because of cement less joint fixture mechanism and design, this endoprosthesis system is able to preserve collateral ligament and adjust the tension of collateral ligament. Twenty-six patients (24 women and 3 men) with average age of 59. 8years(range 35–80 years) were operated. Four patients were operated in both hands. Total of 93 joints were operated in 30 hands, average 3. 1 joints in one hand (4 in 16, 3 in 5, 2 in 5 and 1 in 4).
Follow up averaged 23. 9 (range 14–37) months. The average arc of motion was 47(20–85) ° and extension lag was significantly improved in most cases. Ulnar deviation recurred moderately about 25%, and 2 cases complained pain with flexion contracture. There were 3 dislocations and 2 loosening with fracture of the leg.
Surface type endoprosthesis preserving surrounding soft tissue is the optimal design in large implant arthroplasties. This new finger joints prosthesis provided cement-less joint fixture mechanism and surface type design and preliminary results were satisfactory. Although further follow up and more cases are required, this finger joint prosthesis has proven to be a very good alternative to silicone implant replacement especially for the young patients.
Multiple factors contributing to an elevated risk for dislocation after total hip arthroplasty (THA) have been identified. Patient-related risk factors that have been identified are prior hip surgery, old age and female gender. However, there have been no prospective reports whether inflammatory arthritis (IA) is an independent risk factor.
From January 1996 to December 1999 427 primary total hip arthroplasties were carried out using one type of uncemented prosthesis: a hydroxyapatite coated EPF-PLUS® cup and a SL-PLUS® stem (PLUS Endoprothetik AG, Rotkreuz-CH). A 28 mm. ball head was used in every hip. To evaluate whether IA is a risk factor for dislocation the incidence and cause of early (< 2 year post-surgery) dislocation in IA hips was compared with those carried out for osteoarthrosis (OA). There were 341 THAs in 311 patients with OA and 69 THAs in 59 patients with IA (mainly rheumatoid arthritis) included in this study. The remaining 17 THAs were for various other reasons and excluded from this study.
Statistical analysis of the dichotomous variables was carried out by the chi-square test and the Fisher’s exact test, Student’s t-test was used for the analysis of continuous variables.
Both groups were comparable with respect to the following risk factors: gender, approach (either straight-lateral or anterolateral), position of the acetabular component and experience of the surgeon. Mean age was lower in the IA group than in the OA group: 61. 0 vs 68. 1 years. Furthermore, the incidence of prior hip surgery was higher in the OA group.
The incidence of dislocation was 7 out of 69 (10. 1%) in IA hips and 10 out of 341 (2. 9%) in OA hips (p=0. 006). All dislocations in IA where posterior, in OA 5 were posterior and 4 were anterior (1 unknown). No other mechanical factors leading to an increased instability of the hip in IA, such as trochanteric fractures, could be identified. Due to the relatively small numbers a statistical difference in the direction of dislocation could be identified (p= 0. 088).
So, IA has to be considered as an independent risk factor for dislocation after THA. Both the polyarticular impairments and the lower quality of the soft tissues in IA could explain this elevated risk. To reduce the incidence of dislocation in IA it therefore seems advisable to pay detailed attention the soft tissues and the position of the prosthetic components in IA at the time of surgery. Also, consideration should be given to the use of an acetabular component with an elevated rim.
Total elbow arthroplasty (TEA) is a widely accepted for the treatment for damaged rheumatoid elbows to achieve sufficient joint function. The current prospective study reports the long term follow-up of TEA with an unlinked stem type (Stemmed Kyocera type I, SKC-I) with a solid trochlea on patients who have rheumatoid arthritis (RA). SKC-1 is derived from an unlinked surface replacement prosthesis using polycrystalline alumina ceramics on high-density polyethylene (Kyocera type I), which was developed in 1979, based on the measurement study on the cadaveric elbows.
57 elbows (Larsen’s grade IV and V) from 45 RA patients replaced by SKC-1 were investigated. Cement fixation was used in all cases. The duration of follow-up ranged from 36 to 154 (average 73. 7) months. The clinical condition of each elbow before and after operation was assessed according to the scoring system of Japanese Orthopaedic Association (JOA) elbow scoring system (maximum 100 points), which is composed of scores for pain, activity of daily life, muscle strength, range of motion, instability, and deformity of the joint. On the basis of this system, the results are defined as excellent (90–100 points), good (75–89), fair (60–74), and poor (< 60). Radiographic loosening was defined as a progressive radiolucent line of more than two millimeters that completely surrounded the prosthesis.
The average postoperative JOA score improved from 43. 5±10. 2° to 81. 0±}10. 3°, with marked pain relief. The mean range of motion (ROM) of extension/flexion before the surgery was –35. 7±}22. 4/117. 1±}19. 1° and at last follow-up was −17 5±}12. 7/136. 3±}11. 4°. The mean ROM of pronation /supination improved from 51. 1±}23. 4/56. 5±}28. 5° to 78. 3±}16. 8/82. 3±}16. 5°. Of the 57 elbows, 9 elbows were judged to have excellent results, 37 had good results, 8 had fair results, and 3 had poor results.
There were no instances of ulnar nerve palsy, triceps avulsion, or postoperative infection. Medial or lateral epicondylar fracture occurred in 2 cases during the operation, and union was achieved 3 months later. Massive instability with joint dislocation was seen in 3 cases of mutilans arthritis, resulting in poor results. Aseptic loosening was seen in 3 elbows. Revision surgery was performed in 1 case of accidental post-operative distal humerus fracture, and in another of olecranon fracture with the breakage of the ulnar component. With loosening defined as the end point, Kaplan-Meier curve of the cumulative probability of survivorship demonstrates the likelihood of survival of the prosthesis at 93. 8 percent for as long as 10 years.
The results of the current study showed a high reliability of the SKC-1 prosthesis with the novel alumina ceramic component over a long period when implanted with cement. However, the use of non-constrained devices is limited by the amount of bone and by the need for ligamentous stability. If soft tissues are damaged along with marked bone loss or inflammatory changes, the ligament should be repaired or a semiconstrained type of prosthesis is indicated. It is important to note that a high level of surgical technique is required for TEA in RA elbows to avoid typical postoperative complications.
Total hip arthroplasty (THA) is the only successful treatment for patients in whom the hip joint is destroyed by inflammatory arthritis. Due to the effects of both the disease and its treatment elevated rates of complications and of aseptic loosening have been described. Whether with modern uncemented hip prostheses the results can be improved is not fully known. Therefore, we decided to carry out a prospective study.
At the introduction of a new press-fit acetabular component a prospective study on the results of uncemented THA was started. From 1995 to 1999 85 primary THAs were carried out in 72 patients (57 women, 15 men) suffering from inflammatory arthritis. Diagnosis: RA 76, adult-onset Still 4, JIA 3, miscellaneous 2. Mean age at operation was 60 years (SD 15. 9). Clinically, the Harris Hip Score was used for evaluation. Radiographically, the Larsen classification was used and at follow-up radiolucencies and signs of migration were registered.
The implants used in this study were the EPF-PLUS® acetabular component and the SL-PLUS® femoral component (PLUS Endoprothetik AG, Rotkreuz-CH). The EPF-PLUS® acetabular component is a novel modular press-fit cup. Its shell has a triple radius profile on cross-section, thereby creating a gradual lowering of the polar part of the cup. This produces a small gap of about 2 mm. between the acetabulum and the pole of the cup. Therefore, forces are mainly transmitted to the peripheral part of the acetabulum, leading to an enhanced primary stability. Originally, the shell had a gritblasted surface for osseointegration. Since 1996, the outer surface of the cup has been coated with a ground layer of pure titanium and a superficial layer of a crystalline hydroxyapatite (Ti-HA). The gritblasted version was used in 14 hips (1995–1996), the Ti-HA coated version in 71 hips. In 68 hips the cup was implanted by press-fit fixation, in 17 screws were added.
Larsen classification was as follows: 0-1: 6; 3: 17; 4: 60; 5: 2. At follow-up, 5 patients (6 THAs) were deceased. Deep infection required revision in one hip. Another revision was carried out for recurrent dislocations. One grit-blasted cup developed late subsidence and was revised almost 4 years postoperatively. One Ti-HA coated cup failed early due to severe acetabular bone loss. Finally, one femoral component developed a varus tilt and became symptomatic 2 years after implantation, requiring revision. In all 62 patients with 74 THAs in follow-up cup and stem are functioning well, both clinically and radiographically. Harris Hip Score increased from 36. 6 (SD 17. 7) to 87. 9 (SD 11. 8).
The medium-term results of the EPF®-PLUS cup show that its primary stability is good and that, as the polar gap rapidly disappears, osseointegration is secure. Only severe acetabular deficiency appears to be a contra-indication for this implant. Also, the SL-PLUS® stem performs well in inflammatory arthritis.
In patients with severe acetabular deficiency due to rheumatic arthritis (RA), the mid-term result of THA including a bone graft in the acetabular bed were analyzed.
A total of 32 patients with 40 joints, comprising of 30 females and 2 males, were reviewed in this study. These patients had severe acetabular deficiency and were receiving THA for RA, including a bone graft in the acetabular bed. The average age at surgery was 58. 3 years and the average follow-up period was 6. 2 years. These patients had suffered from RA for 21 years on an average. The acetabular bed was filled with the chip bone and covered with the slice bone, followed by strong pressurization of the implanted bone and fixation of the cup with a screw. The patients were evaluated clinically using the Harris hip score, and radiologically using the Gruen radiographic analysis and the Sotelo-Garza and Charnley classification.
In the clinical evaluation using score, the mean score improved from 39. 7 preoperatively to 82. 3 postoperatively. An improvement in pain, walking ability, ROM and ADL were observed. In the radiological evaluation using the Gruen analysis, more radiolucent lines tended to appear in the zone 1, of which none was progressive or indicated loosening. On the femoral side, more partially radiolucent lines of 1 mm or less tended to appear in the zone 4, of which none indicated osteolysis or loosening. The mean thickness of acetabular bed improved from 4. 3 mm preoperatively to 13. 5 mm postoperatively. During the follow-up period, no collapse of the implanted bone, dislocation of the cup or loosening was observed.
Treatment with the bone graft method using slice bone and chip bone are used for acetabular deficiency in rheumatic hip joint in our department, this methods is considered to be an effective treatment, because it has provided a good initial fixation of cup and a good graft survival.
The wrist is the ”key-stone” of hand function. Painless stability is a prerequisite for the rheumatoid wrist to perform various manual tasks. Synovectomy of the extensor tendons and the wrist joint with a Darrach procedure is offered for painful wrists, which are not controlled by conservative treatment with medication and orthosis. Radiolunate arthrodesis is performed on wrists with an unstable radiocarpal joint and preserved midcarpal joint space. This study describes the long-term (more than 10 years) follow-up of these operative procedures.
The follow-up study was performed on 25 wrists in 25 rheumatoid patients (22 women and 3 men), whose average age was 52 years (range, 33 to 66 years) with an average disease duration of 12 years (range, 1 to 38 years). The average follow-up period was 12. 5 years (range, 10 to 18 years). Five wrists were Larsen-Dale-Eek’s grade II, 14 were grade III, and 6 were grade IV. Depending on the severity of bone destruction, the scaphoid in 6 wrists and the triquetrum in 3 wrists were included in the fusion site.
Preoperative pain (88%) and swelling (96%) decreased remarkably at follow-up (12%, 4%). Average grip strength increased significantly from 100mmHg to 140mmHg (p< 0. 01). The total arc of wrist extension/ flexion decreased to two-thirds of the preoperative arc with a major loss in flexion (preop. : 26/28degrees, follow-up: 23/13degrees). The range of forearm rotation increased due to a Darrach procedure. In periodical X-ray assessments of 23 wrists, carpal collapse initially improved following the operation, however, it returned to the preoperative level after 5 years. Ulnar carpal shift improved significantly after the operation (p< 0. 01), and the position remained unchanged over 10 years. In palmar carpal subluxation, no remarkable change was noted. Bone union occurred in 87% of the operated wrists and the remaining 13% had fibrous union. Widening at the lunocapitate joint (> 2mm) was noted in 4 wrists (17%) and progressive instability at the midcarpal joint occurred in one wrist with the mutilating type of disease. Narrowing (< 1mm) was noted in 5 wrists (22%) and 3 wrists were totally fused in the functional position.
Radiolunate arthrodesis provides good stability with some motion for the moderately deteriorated rheumatoid wrist more than 10 years after the operation, in spite of some radiological progression of the disease. This operation is considered to convert the natural course of the rheumatoid wrist from the unstable form to the stable form.
Since 1981, we have used various types of the total hip prosthesis for the reconstruction of the acetabular protrusion in rheumatoid arthritis. The cemented Charnley prosthesis was used during the initial 8 years, and we experienced loosening of the cemented acetabular socket in some cases. The bipolar femoral head prosthesis, which started to be used from 1984, was one of the cementless prosthesis. And it showed high frequency of proximal migration of outerhead. The threaded socket also showed frequent loosening. To overcome these problems, we started to utilize a new method from 1988. This method included packing morselized bone grafts into the acetabulum and fix them using a porous coated socket and screws. This study describes the results of cementless total hip arthroplasty (THA) for the acetabular protrusion in rheumatoid arthritiswith this method.
Sixty -one cementless THAs with use of porous coated acetabular socket were performed in 50 patients who had sever protruded acetabulum due to rheumatoid arthritis. The average follow –up period was 9 years and 5 months (range, 5 to 13 years). A Mallory/ Head prosthesis with porous coated socket was used in 43 hips and other types in 18 hips. In all operated hips, autogenous morselized bones were grafted on the thin acetabullar wall.
The clinical improvement in pain was the most apparent. X-ray findings of the grafted bone in the acetabulum showed a homogenous pattern in most cases (90. 2%) at 6 months after the operation. A radiolucent zone at a non-weight-bearing area between the grafted bone and socket was seen in 20 hips (32. 7%) for 3 years after the operation, and it gradually disappeared and changed to a sclerotic zone. Collapse and /or absorption of the grafted bone were noted in 3 hips of the patients with sever osteoporosis and high disease activity.
There are several technical key points to succeed THA in patients with rheumatoid arthritis. The first is the selection of the acetabular socket. The second is the method of bone grafting, and the third is the size and the shape of grafted bones. We have used various types of prosthesis for the protruded acetabulum so far, and it was considered that the bipolar and threaded types are not acceptable because of their high frequency of proximal migration and loosening. The mass and /or block bone should not be used, because they are liable to fall into collapse. It is safely recommended to use slice or morselized bones to lead the grafts to early survival and remodelling caused by tight and close contacts.
THA with the use of morselized bone grafting into the acetabulum and a fixation with a porous coated socket-and screws is a simple and useful procedure for treating protruded acetabulum in rheumatoid arthritis.
Schoulder function in the rheumatoid patient is often restricted by pain and the decrease of range of motion, muscle strength and coordination. The aim of treatment in particular joint replacement is to improve one or more of these factors to enhance shoulder function. It is unknown how much range of motion of the shoulder and the glenohumeral joint is actually needed after shoulder replacement for a reasonable function.
The shoulder function of 114 rheumatoid patients (28 male and 86 female) with a shoulder replacement was pre- and post-operatively scored at regular intervals with the Constant scale and the HSS scoring system. These scoring systems measure the ROM and daily functioning. Activities of daily living used were: dress, comb hair, wash opposite axilla and use toilet and these items were scored numerically (5=normal, 0=impossible). These items were correlated with the active ROM of the shoulder and the passive ROM of the glenohumeral joint. The passive ROM of the glenohumeral joint included the ab/adduction movement in the frontal plane, the rotation in resting position and the exorotation in 90° anteflexion. 54 Patients had a hemi-arthroplasty and 60 patients had a total shoulder prosthesis. The average follow-up was 5 years.
The average active ROM measured at follow-up was: flexion 81°±36; abduction 70°±27; exorotation 21°±23. The average passive glenohumeral motion was: exorotation in 90° flexion 42°±33; ab/adduction 51°±21; rotation 61°±30. The average functional score of the activities of daily living measured were: comb hair 2. 8±1. 9; toilet use 3. 9±1. 6 and wash opposite axilla 4±1. 5. There was a significant relationship between flexion/rotation and the functional task comb hair. The other activities of daily living were not significantly related with ROM of the shoulder. The minimal range of motion for optimal functioning of the shoulder was calculated.
Exorotation of the 90° flexed shoulder appears to be the most important parameter for an optimal functioning after shoulder prosthesis.
Synovectomy in children with juvenile rheumatoid arthritis (JRA) and psoriatic arthritis (PSA) is still subject of controversial discussion. Our results of arthroscopic synovectomy of the knee in children with chronic inflammatory joint disease are presented.
From 1989–1997 27 synovectomies were performed in 27 children with inflammatory arthritis (15 JRA, 12 PSA). Average age at surgery was 12. 5 y (2. 9–17. 8 y). Mean follow-up was 4. 9 years.
Onset of disease and conservative therapy was documented. Each patient was physically and radiologically examined preoperatively and 24 children postoperatively (mean follow-up 4. 9 years). For arthroscopic shaver-assisted synovectomy of the knee we used minimum 4 portals and normally 6 portals (2 anterior, 2 suprapatellar and 2 posterior portals). In addition to the physical examination we used a special clinical score (Laurin 1974). We compared the pre- and postoperative limits of active and passive knee movement. We performed sonographs and radiographs of the infected joint. Radiography was classified following the Larsen-Scale. Patient and parents gave their opinion whether the operation was successful. Before surgery all children had intensive drug and physical therapy for 8–62 months (42 month). In the course of conservative treatment, knees had local joint treatment with triamcinolonhex-acetomid (THA), normally for three times before surgery. Preoperative X-rays showed Larsen stage I in 3 knee joints and Larsen stage 0 in the other knees.
In 85% of the children, we found good or excellent surgical outcome. 2 joints achieved fair and 2 joints poor outcome. Concerning subjective outcome 22 (82%) children had been very satisfied (56%) or satisfied (26%). 25 of the children’s parents would agree in the same surgical procedure again. In 6 knee joints we found recurrent synovitis. 2 of these knee joints were reoperated (30 and 22 month postoperatively with satisfying result), the other 4 joints were treated with THA i. a.. The 2 reoperations were regarded as poor result. We had no postoperative complications and the normal hospitalisation was 15 days. Prior to surgery, 12 knee joints had an average deficit of active knee extension of 10° (5–20°). Postoperatively, no extension deficit was found anymore in 25 of the knees. Compared to the contralateral knees, a flexion deficit of 10° (5–15°) was obtained postoperatively. At sonography, no joint effusion could be revealed. Postoperative X-rays showed no progression in Larsen stage. Outcome in children with oligoarthritis was better than in those with polyarthritic disease.
Early arthroscopic synovectomy of the knee in children with chronic inflammatory joint disease is, in case of failure of conservative treatment, a useful method of treatment. We propose early synovectomy of the knee joint as an essential part of the treatment scheme for children with inflammatory joint disease.
Destruction and deformity in both PIP and MP joints are not uncommon and cause sever disabilities. Arthroolasty of the MP joint combined with arthrodesis of the PIP joint are the usual choice for this condition. Some motion in ulnar digits provides great benefits for rheumatoid patients. We report implant arthroplasty of the PIP joint and also simultaneous replacement of PIP and MP joint in same finger.
Twenty-five joints in 15 patients underwent PIP arthroplasty either with silicone or surface replacement implant. Twelve PIP joints in 6 patients used Silicone implant (6 Swanson and 6 Avanta) alone and mean follow up was 42(6–84) months. New cementless surface implant (Self Locking Finger Joint, SLFJ) were developed and clinically used for about 3 years. Because of the stem design, SLFJ are able to use both PIP and MP joint simultaneously or combined with silicone implant. Four PIP joints in 3 patients used SLFJ alone and 6 patients underwent both PIP and MP joint with implant simultaneously. Combination of SLFJ PIP and silicone MP was 4 finger in 2 hand, SLFJ PIP and SLFJ MP was 3 finger in 2 hand, silicone PIP and SLFJ MP was 3 finger in 2 patients and silicone PIP and silicone MP was 1 finger. Mean follow up for SLFJ in either PIP or MP was 18(4–37) months.
Average arc of the PIP with silicone implant alone was 38(10–50 ° and SLFJ alone was 55(45–60) °. One PIP SLFJ dislocates immediate after surgery and was converted silicone later on. Of 7 SLFJ with combined PIP and MP arthroplasties, 2 PIP lost motion completely, one PIP move only 15°, 4 PIP move 75 °in average. Four silicone PIP combined with MP arthroplasties move 45°in average.
One PIP SLFJ had breakage in stem legs, which believed to occur during interaction of stem insertion from both side of the basal phalanx, and was seen at immediate post op X-ray. There was one instability in index replaced with SLFJ for sever Swan neck deformity and no infection. Patient satisfaction for simultaneous replacement in PIP and MP joint were excellent except one whose age was 72.
Stability of the PIP joint in index finger is important for pinch and PIP motion of ring and little fingers are required for grip motion. Although arthrodesis of the PIP joint were performed more often and functional improvement usually obtained compared to pre-operative condition, ulnar 2 digits better to preserve some motion in the PIP joint as long as there is a possibility, and especially for the young patients. The results of the simultaneous replacement in PIP and MP joint seems discourage, however, when considering the severity of the deformities of this series, there is a good chance in the future. We will improve implant design and surgical technique as well as post-operative therapy, and continue to challenge the simultaneous replacement of PIP and MP joint.
The wrist is the ”key-stone” of hand function. Painless stability is a prerequisite for the rheumatoid wrist to perform various manual tasks. Synovectomy of the extensor tendons and the wrist joint with a Darrach procedure is offered for painful wrists, which are not controlled by conservative treatment with medication and orthosis. Radiolunate arthrodesis is performed on wrists with an unstable radiocarpal joint and preserved midcarpal joint space. This study describes the long-term (more than 10 years) follow-up of these operative procedures.
The follow-up study was performed on 25 wrists in 25 rheumatoid patients (22 women and 3 men), whose average age was 52 years (range, 33 to 66 years) with an average disease duration of 12 years (range, 1 to 38 years). The average follow-up period was 12. 5 years (range, 10 to 18 years). Five wrists were Larsen-Dale-Eek’s grade II, 14 were grade III, and 6 were grade IV. Depending on the severity of bone destruction, the scaphoid in 6 wrists and the triquetrum in 3 wrists were included in the fusion site.
Preoperative pain (88%) and swelling (96%) decreased remarkably at follow-up (12%, 4%). Average grip strength increased significantly from 100mmHg to 140mmHg (p< 0. 01). The total arc of wrist extension/ flexion decreased to two-thirds of the preoperative arc with a major loss in flexion (preop. : 26/28degrees, follow-up: 23/13degrees). The range of forearm rotation increased due to a Darrach procedure. In periodical X-ray assessments of 23 wrists, carpal collapse initially improved following the operation, however, it returned to the preoperative level after 5 years. Ulnar carpal shift improved significantly after the operation (p< 0. 01), and the position remained unchanged over 10 years. In palmar carpal subluxation, no remarkable change was noted. Bone union occurred in 87% of the operated wrists and the remaining 13% had fibrous union. Widening at the lunocapitate joint (> 2mm) was noted in 4 wrists (17%) and progressive instability at the midcarpal joint occurred in one wrist with the mutilating type of disease. Narrowing (< 1mm) was noted in 5 wrists (22%) and 3 wrists were totally fused in the functional position.
Radiolunate arthrodesis provides good stability with some motion for the moderately deteriorated rheumatoid wrist more than 10 years after the operation, in spite of some radiological progression of the disease. This operation is considered to convert the natural course of the rheumatoid wrist from the unstable form to the stable form.
The value of the preoperative radiograph of the rheumatoid shoulder is underestimated for defining the moment for arthroplasty. Larsen grades 4 and 5 are widely used as radiological criterium, but this grading system is not sufficient for staging important surgical aspects as proximal migration and medialisation of the humeral head. The purpose of this study is to analyse the proximal migration and medialisation in severely destructed shoulders (Larsen 4 and 5) and to correlate this with the clinical and per-operative findings to optimize the timing for shoulder arthroplasty.
From a large group of patients with a shoulder arthroplasty those were selected who had preoperatively an involvement of the shoulder graded as Larsen 4 or 5. 104 Rheumatoid patients were selected (29 male, 75 female). The average age was 60 years (range 25–83 yrs). All patients were preoperatively clinically scored with the HSS-score, a 100 points scoring system, which assesses pain, function, power and range of motion. The radiographs were scored for the following items: gleno-humeral joint space, bone loss of glenoid, destruction of the humeral head, proximal migration and involvement of the AC-joint. The most important peroperative items were the quality of the rotator cuff and the glenoid bone mass.
69 Shoulders were graded as Larsen 4 and 35 as Larsen 5. Medialisation by bone loss of the glenoid was moderate in 65% and severe in 13. 6% of the shoulders. Proximal migration was moderate in 22% and severe in 39% of the shoulders. There was no significant correlation between medialisation and proximal migration. The rotator cuff was torn in 44% of the shoulders. Although a torn cuff was significantly related with proximal migration there were many cases with maximal proximal migration with an intact cuff. The clinical scores were not significantly related with the radiographic deterioration of the shoulder.
Because of the discrepancy between clinical findings and radiographic destruction of the rheumatoid shoulder, the radiographic findings have to play a more important role in the indication of shoulder arthroplasty to achieve a better functional and long-term result.
Matrilin-3 is a member of the recently described matrilin family of extracellular matrix proteins containing von Willebrand factor A-like domains. The matrilin-3 subunit can form homotetramers as well as hetero-oligomers together with subunits of matrilin-1 (cartilage matrix protein). It has a restricted tissue distribution and is strongly expressed in growing skeletal tissues. Detailed information on expression and distribution of extracellular matrix proteins is important to understand cartilage function in health and in disease like osteoarthritis.
Matrilin-3 expression was analysed on decalcified normal cartilage/bone sections (N = 5) and decalcified cartilage/ bone sections with minor (N= 10), moderate (N = 10), and severe osteoarthritic lesions (N = 10). Osteoarthritic changes were classified histomorphologically, using the grading system of Mankin. Matrilin-3 expression was investigated by immunohistochemistry, in situ hybridization, Western blot analysis, and quantitative PCR. For immunohistochemistry, a polyclonal antibody against matrilin-3 was used. For Western blot analysis, cartilage extracts were obtained from normal and osteoarthritic samples, partially purified, and separated in SDS poly-acrylamide gelelectrophoreses. After blotting onto nitro-cellulose, matrilin-3 was visualized by incubation with the polyclonal anti-matrilin-3 antibody and chemiluminescence detection. Matrilin-3 -mRNA expression was determined by in situ hybridization using a digoxigenin-labeled anti-sense probe.
Our results indicate that matrilin-3 is a mandatory component of mature articular cartilage with its expression being restricted to chondrocytes from the tangential zone and the upper middle cartilage zone. Osteoarthritic cartilage samples with only moderate morphological osteoarthritic destructions have elevated levels of matrilin-3 mRNA. In parallel, we found an increased deposition of matrilin-3 protein in the cartilage matrix. Matrilin-3 staining was diffusely distributed in the cartilage matrix, with no cellular staining being detectable. In cartilage samples with minor osteoarthritic lesions, matrilin-3 deposition was restricted to the middle zone and to the upper deep zone. A strong correlation was found between enhanced matrilin-3 gene and protein expression and the extent of tissue damage. Sections with severe osteoarthritic destruction showed the highest amount of matrilin-3 mRNA, strong signals in in situ hybridization, and prominent protein deposition in the middle and deep cartilage zone.
We conclude that matrilin-3 is an integral component of human articular cartilage matrix and that the enhanced expression of matrilin-3 in osteoarthritis may be a cellular response to the modified microenvironment in the disease.
Total endoprosthetic replacement of hip and knee joints in patients with degenerative or inflammatory disease is a reliable treatment in orthopedic surgery since many years.
However patients with oligo- or polyarticular disease are still a problem because of several operations within repeated periods of hospitalisation. Patients who need multiple joint replacements reject surgical procedures considering long time of suffering and hospitalisation by being treated in following one step after the other. Offering simultaneous surgery in two joints is often a probate opportunity to avoid this problem. To resolve this problem we decided one stage procedure in selected cases.
Between 01. 01. 99 and 31. 12. 01 we supplied 57 patients with 2 endoprosthesis (hip or knee) in one single surgical procedure.
In 26 cases we implanted total hip replacement bilateral. 11 patients were female and 15 patients were male. The age differed between 26 and 73 years with an average of 64 years. One patient got hybridendoprosthesis (Muenchner socket/MEM stem). The others got a cementless model (Fitek or ACA socket/Weill or Spotorno stem). The average time of hospitalisation was 23, 5 days. In 3 cases allogenic packed human bloodcells (up to 960 ml in one case) were necessary. The mean time of operation was 142 min.
In 25 cases we did total knee alloarthroplasty on both sides. 17 patients received all cemented Wallaby-I knees and 1 patient received all cemented PFC prosthesis. 7 patients got got an all cemented Scorpio knee prsthesis. 14 of these patients were female and 11 patients were male. The age differed between 35 and 75 years with an average of 66. The average time of hospitalisation was 21, 5 days and the average time of operation took 123 min. Allogenic packed human bloodcells were not necessary in any case.
In 6 cases we did total alloarthroplasty on knee and hip simultaneous. All patients received all cemented Wallaby-I knees and different cementless or hybrid-hip-prosthesis (Fitek or ACA socket/MEM, Weill or Spotorno stem). 4 of these patients were female and 2 patients were male. The age differed between 39 and 79 years with anaverage of 61. The average time of hospitalisation was 24, 5 days. The mean time of operation was 132 min. Transfusion of allogenic packed human blood-cells was necessary in one case.
By standard all patients underwent praeoperative blood donation and postoperative autologous retransfusion (mean 640 ml) within 6 hours.
In four cases we saw an increase of the inflammatory test results one week postoperative, which we treated with Tavanic 500 1 - 0 - 0 orally. Other complications didn′t occur. All patients were able to leave the hospital with full weight bearing.
Compared to single hip joint replacement the average time of hospitalisation was only 4, 1 days longer, in case of simultaneous knee replacement we saw an increase of 3, 3 days.
Considering the high acceptance due to the above mentioned advantages we recomand simultaneous replacement of two joints as an approbiate procedure in patients suffering from multiple joint destructions.
Mechanical loading has been hypothesized to play an important role in the development, remodeling and in diseases of many skeletal tissues, including cartilage. In order to study the metabolic response of cartilage to physical forces, in vitro systems have often been used because of the precise control with which mechanical loads can be applied. We developed a new mechanical loading system, in which we were able to load the intact femoral condyle in order to preserve the native cartilage/subchondral bone structure. This system represents a more ‚in vivo‘ situation than cartilage explants or chondrocyte cell culture systems.
Our approach focused on changes in mRNA expression of type II collagen, type VI collagen, and aggrecan in loaded versus adjacent unloaded cartilage in order to analyse the early response of chondrocytes to well-defined mechanical stresses.
Femoral condyles were obtained from two-year-old cows. The integrity of the cartilage surface was controlled by staining with safranin O. The femoral condyles were compressed in an Instron 8501 material testing machine. Cyclic compression pressure was applied for 2000 cycles in a sinusoidal waveform of 0. 5 Hz-frequency with a peak stress of 0. 2 to12. 5 MPa. Following loading, full depth cartilage sections were cut out and one half immediately frozen in liquid nitrogen for RNA isolation and the other half soaked in 4% paraformaldehyde for paraffin embedding. As control, the adjacent unloaded cartilage was collected and treated in the same way. Total RNA was isolated and changes in mRNA expression were quantitated by competitive quantitative PCR, using an internal standard of a C-terminal truncated version of the corresponding genes. The PCR-reactions were separated by agarose gel electrophoresis and amplified fragments quantified using video-densitometry analysis. The results were expressed as the ratio of mRNA from loaded to unloaded cartilage
Cyclic compression with peak stresses of 12. 5, 6. 3, 2. 5 and 0. 6 MPa lead to a two-fold decrease in the mRNA expression of type II collagen and aggrecan and a threefold decrease of type VI collagen, in consideration of the intra-assay variability of about 30%. Compression with peak stresses of 0. 3 and 0. 2 MPa lead to a three-fold increase of the mRNA expression of type II collagen, a four-fold increase of aggrecan and a slight decrease of type VI collagen.
Low compression strength leads to an increase of the mRNA expression of the major components of cartilage, type II collagen and aggrecan, whereas high loading leads to a decrease of the mRNA expression.
The results show that our system can be used to analyze early responses of chondrocytes to well-defined mechanical stresses in an intact cartilage/bone-system and therefore will enable us to investigate the role of physiological and non-physiological high loading on the induction of cartilage degradation and regeneration in joint trauma and osteoarthritis. Since the cartilage/bone samples are incubated in medium during the experiment, this system will also offer us the opportunity to investigate additives to the medium as potential pharmacological therapeutics in osteoarthritis.
In rheumatoid patients the use of a long intramedullary stem in ipsilateral shoulder and elbow replacement carries the risk of humeral fracture of the small area of unviolated bone between the implants. Healing may be compromised. Because of this a short stemmed humeral head prosthesis was designed which rests on the bone surface after resection of the humeral head instead to be fixed in the shaft of the humerus. Since 1994 this prosthesis, specially designed for the rheumatoid patients has been in use in our clinic. The design rationale and the clinical results will be presented.
Since 1994 the short stemmed shoulder prosthesis has been inserted by the author in 54 shoulders.
8 Patients had osteoarthritis, 42 patients rheumatoid arthritis, 3 patients osteonecrosis and 1 patient a post-traumatic osteoarthritis. The average age was 65 years (range 32–83). In 19 shoulders a total shoulder arthroplasty was performed and the 36 shoulders a hemiarthroplasty. 32 Patients had a follow-up of more than 1 year and the average follow-up in this group is 2. 5 years (range 1-5. 5).
All patients were scored clinically with the HSS score and the Constant score and radiographically before the operation, 1 year after the operation and after that at regular intervals. At follow-up pain decreased in all patients but more than 50% of the shoulders still had some mild or moderate pain during daily activities. Pre-operatively active forward flexion averaged 61°, external rotation 10° and abduction 50°. Postoperatively the active forward flexion increased to 75°, the external rotation to 19° and the abduction to 67°. The gain in ROM is similar to a group of patients operated in the same time period with another shoulder prosthesis.
The short stem shoulder prosthesis is a good alternative for a shoulder prosthesis with a long intra medullary stem. The clinical results with regards to pain reflief and gain in ROM are similar. The long term fixation of short sem humeral prosthesis remains good, without signs of radiolucency or migration. The advantage of a short stem prosthesis are:
easy technique to reconstruct the anatomical position of the humeral head bone sparing no stress shielding of the shaft no surgical problems when a long stemmed elbow prosthesis is used possibility for revision
The interposition arthroplasty using dura mater has been applied by us as an alternative method to implantation of the prosthesis since 1997. This new surgical method was developed on the basis of ulnohumeral arthroplasty according to Kashiwagi to aspire to preserve the integrity of the joint. We used for interposition instead of lyophilized dura mater the Tutoplast° dura graft, which is treated with osmotic solvent and in this way differs from the lyophilised graft, as its tensile and pulling strength is greater, since it preserves its collagen structure and its three-dimensional fibrin structure.
The dura mater interposition was applied with 23 patients in 24 cases (one bilateral), from May 1997 up to July 2000, in 17 occasions on the dominant side. The average age of the patients was 52. 2 years (24–75 years). The basic diagnosis was rheumatoid arthritis in 83. 3 percent, juvenile chronic arthritis in 8. 3 percent and post-traumatic osteoarthritis in 8. 3 percent. All the patients appeared at the follow up examination and the average duration of the follow-up was 26. 6 months (from 8 to 45 months). The clinical evaluation was based on the Mayo performance score.
Praeoperatively 71 percent of the twenty four patients had severe pain, while none of them had it at the follow up examination. 50 percent of patients were painless, 29. 2 percent had moderate and 21 percent of them had mild pain. The average decrease of point of Mayo performance score for pain was 5. 8 points, the difference is significant (p< 0. 001).
Increase of range of movement is also remarkable. Praeoperatively only 4. 2 percent of the twenty four patients had an arc of 100 degrees or more, at the follow up examination this proportion improved to 66. 7 percent. Mean value of the increase was 28. 5 degrees, the difference is significant (p< 0. 001). Range of motion of supination and pronation improved significantly (p< 0. 001).
Sixty seven percent of our patients were stable prae-operatively, this value decreased to 50 percent at the follow up. Grossly instability was observed 21 percent praeoperatively and 33 percent at follow up examination. Mean decrease of stability was 4. 2 degrees, the difference is significant (p< 0. 026). We have to notice at the same time that five of the eight grossly unstable patients had the same measurement of instability prae-operatively too, two had moderate instability and only one of them was stable before operation.
The quality of life – as far as the basic vital functions are concerned- improved with 91. 6 percent. It is very important to notice at the evaluation of Mayo performance score that 95. 8 percent of patients falled to the group with poor classification before operation, but this value decreased to 12. 5 percent at the follow up, moreover 50 percent of patients had excellent and 79. 2 percent had excellent or good classification. Mean increase of Mayo performance score evaluated to 53. 2 points, the difference is significant (p< 0. 001).
One of the most serious complication of interposition arthroplasties is the absorption of the bone structures. Hence we mainly observed the radiological signs of this and employed the evaluation method of
On the basis of the short-term clinical and radiological results the interposition using dura mater as an alternative way to the implant arthroplasty, may be applied with good results.
In rheumatoid arthritis, the forefoot is frequently affected. A variety of surgical procedures have been established in the treatment of rheumatic forefoot disorders. Postoperatively, patients are mobilized in specially designed footwear to reduce forefoot stress. Our study was conducted to investigate peak and mean plantar pressure occurring in two differently designed forefoot relief shoes by using the novel pedar ® system.
Ten symptom-free volunteers were asked to walk on a treatmill, performing two trials at self-selected speed. The ”Barouk” (sole and heel supporting proximal fifty percent of the foot) and “Hannover” (Sole under whole foot, heel supporting proximal fifty percent of the foot) forefoot relief shoe (fior and gentz, Lueneburg, Germany) were compared. In a first trial, the shoe had to be used adequately, while in a second trial, the volunteers tried to put pressure on the forefoot, mimicking non-compliance. Peak and mean plantar pressure were obtained using the pedar® cable system (novel, Munich) and compared to the contralateral foot. Statistical t-test analysis was performed using SPSS 10. 0 for windows™.
When wearing the “Barouk” shoe with short sole, the forefoot was completely relieved in all trials. Non-compliant use of the shoe did not result in any forefoot stress. At the edge of the sole, peak pressure values were not higher than in conventional footwear. The shoework with complete sole reduced forefoot peak and mean pressure in contrast to normal gait by a mean of 34 percent. However, all volunteers were able to put stress on the forefoot when mimicking non-compliance, reaching peak values similar to normal gait.
With regard to reconstructive forefoot surgery, the design of forefoot relief shoework affects the safety to non-compliance.
The radiographs of sixty-four patients with seventy humeral head replacements were reviewed for signs of stress shielding. Forty-nine were implanted for rheumatoid arthritis, twenty-one for osteoarthritis. The radiographic follow-up averaged 5. 3 years. Measurements of cortex thickness were performed in four regions along the stem of the implant and the differences between the post-operative radiograph and radiograph at follow-up were calculated. The size of the stem in relation to the diameter of the humerus was calculated using validated measures, resulting in the relative stem size.
A reduction of 1.6 millimeters or more was considered to be a significant reduction, because this lay outside of the calculated 95% normal range for the group as a whole. In six patients (9%) a significant reduction, in cortical thickness was observed in the proximal lateral region of the humeral stem. Five of these had rheumatoid arthritis and one osteoarthritis. In the stress shielding group the relative stem size was found to be significantly higher (p=0. 013) than in the non-stress shielding group (0. 58 versus 0. 48). Osteoporosis, especially present in rheumatoid arthritis, could well be a risk factor. It was concluded that stress shielding is a long-term complication of shoulder arthroplasty and that the relative stem size is an important factor in its genesis. These resorptive processes may lead to a higher risk of failure of the implant and gives an increased risk for mid-stem fractures, due to cantilever loading. It is also desirable to preserve the proximal bone stock, considering the difficulties that arise when, for whatever reason, revision of the implant is necessary.
A 18-year-old woman patient suffering from JCA was operated on non-dominant left shoulder joint destruction. The dysplasia of the affected side was clearly recognisable on the X-ray befor the operation as compared to the other side. The smallest of the prothesis typs (De Puy Global, Biomet Modular) couldn’t be implanted. So we have used an other method.
We have achived good results for years by using Tuto-plast‚ Dura mater (Tutogen Medical GmbH) in operating interposition elbow arthtroplasty of RA patients. This was the basic idea in this case to apply shouldes joint interposition arthroplasty. There have been previous publications on other interposition tecniques.
Traditionally we approached the shoulder in deltopectoral sulcus. After the subscapular muscle tenotomy subtotal synovectomy happened, later pannus and osteophyts were removed from the humeral head. Then the surface of the head was refreshened, then arronund the anatomic neck titanium screws ( ORFI-II‚ anchor, Technomed) were placed and Tutoplast placed on the head was anchored to them.
There are no shouldes pains 4 years after the operations, no radiologcal progression can be experienced. The range of motion is under the mesured value of the RA group of patient having shoulder prothesis. Despice of this fact the patient is able to look after herself and do the daily routine. The patient is fully satisfied with the operation.
Althaugh important conclusion can’t be drawn from one case but sometimes it gives a good alternativ solution in the area of prothetics in shoulder dysplasy of different origins.
The incidence of loosening of a cemented glenoid component in total shoulder arthroplasty, detected by means of radiolucent lines or positional shift of the component on true antero-posterior radiographs, has been reported to be between 0% to 44%. These numbers depend on the criteria used for loosening and on the length of follow-up. Radiolucent lines are however difficult to detect and to interpret, because of the mobility of the shoulder girdle and the obliquity of the glenoid, which hinder standardisation of radiographs. After review of radiolucencies around cemented glenoid components with a mean follow-up of 5. 3 years in 48 patients we found progressive changes to be present predominantly at the inferior pole of the component. This may hold a clue for the mechanism behind loosening of this implant. Since loosening is generally defined as a complete radiolucent line around the glenoid component and is difficult to assess as a result of the oblique orientation of the glenoid, an underestimation of the loosening rate using radiological data was suspected. Therefore a pilot study using Roentgen Stereophotogrammatric Analysis (RSA) was performed.
In five patients an additional analysis of glenoid component loosening using digital Roentgen Stereophotogrammetric Analysis (RSA) was performed. The relative motion of the glenoid component with respect to the scapula was assessed and the length of this translation vector was used to represent migration. Loosening was defined as a migration of the component, exceeding the pessimistic estimate of the accuracy of RSA 0. 3 mm for this study. After three years of follow-up, three out of five glenoid components had loosened (1. 2 – 5. 5 mm migration). In only one patient with a gross loosened glenoid, the radiological signs were consistent with the RSA findings. It was concluded that when traditional radiographs are used for assessment of early loosening, the loosening rate is underestimated. We recommend that RSA be used for this.
To investigate the responsiveness to change of four different elbow-scoring instruments, two Hospital for Special Surgery (HSS) elbow assessment scales, the Mayo Clinic elbow-performance index (Mayo) and the Elbow Functional Assessment (EFA) scale.
A group of 24 RA patients (median age 60 years) undergoing either elbow arthroplasty (22 elbows) or synovectomy with radial head excision (3 elbows), were evaluated both prior and after surgery (median: seven months postoperatively). Score changes, obtained by using the scales under study, were calculated. The patient’s opinion of global perceived effect of the intervention was used as a criterion to classify them as ‘improved’ or ‘non-changed’. Responsiveness was evaluated with use of three approaches: using paired t-statistics (pre- and post-surgery scores), effect size statistics (standardized response mean, effect size and responsiveness ratios) and Receiver Operator Characteristic (ROC) curves.
Each of the elbow rating measures under study proved to be responsive to change when evaluating RA patients undergoing elbow arthroplasty or synovectomy. The EFA scale demonstrated the highest power to detect a clinically meaningful difference and had the best discriminative ability to distinguish improved from non-changed patients, as was revealed by all responsiveness statistics applied.
The HSS, the Mayo and the EFA elbow-scoring scales can all be used as an evaluative instrument to assess the efficacy of surgical treatment of the rheumatoid elbow joint. However, using the EFA scale will require smaller sample sizes to achieve a fixed level of statistical power than the other scales under study.
The aim of this study was on the one hand to compare the fixation of a posterior stabilised prosthesis (PS) and a PCL retaining mobile bearing design (Interax, How-medica Osteonics, Rutherfort, USA) and on the other hand to measure the mobility of the mobile bearing. All measurements were carried out by means of Roentgen Stereophotogrammetric Analysis (RSA-CMS, Medis, Netherlands).
Thirty-three patients with a total of forty-two consecutive primary cemented TKA were included in a prospective, randomised study at Leiden University Medical Centre. There were no significant differences among the two groups with regard to age (66. 5 ± 12. 1 years). The pre-operative Knee Society Score did not differ significantly between the two groups. At the one-year follow-up the PS group showed a significantly lower function score (p=0. 04) compared to the mobile bearing group.
At the one-year follow-up evaluation, the micromotion of the PS-components and the mobile bearing components were not significantly different. The PS-tibial components subsided −0. 003 ± 0. 192 mm and the mobile bearing knee tibial components subsided 0. 057 ± 0. 082 mm. The PS tibial component showed a higher variability in the migration results indicating a number of PS with rather large micromotion.
For three patients, the
The wide range of kinematic patterns of mobile bearings during flexion that is observed in fluoroscopic studies is also observed in this study. A possible positive effect of mobile bearing movement may be found in the smaller variability of the micromotion of the mobile-bearing knees compared to the PS knees. The assumption was that shear forces in tibial bones implanted with a mobile bearing prosthesis would be better dissipated from the prosthesis-bone interface resulting in less micromotion. The kinematics of an additional number of mobile bearing knees -already included in the micro-motion study- will have to be assessed in order to determine the relation between mobility and micromotion.
Mobile bearing, Posterior Stabilised, RSA, Kinematics
Survivorship analysis was performed on 479 Link V-Type cementless threaded acetabular cups on 310 cases with inflammatory arthritis, 138 cases with osteoarthritis and 31 cases with dysplastic hip. The average follow-up was 8. 6 ± 3. 2 years. The same analysis was performed on a modified cup with a smaller primary coil (type ”Bad Bramstedt”). This analysis had a mean follow-up period of 4. 5 ± 0. 7 years in 110 cases, including 49 with inflammatory arthritis, 49 with osteoarthritis and 12 with dysplastic hip. In a second approach 264 Link V-cups with a mean follow-up period of 8. 2 ± 2. 7 years and 59 modified cups with a mean follow-up period of 4. 6 ± 0. 7 years were radiologically examined for radiolucent lines according to Delee and Charnley and cup migration with regard to the method of Nunn et al.
The cumulative survival rate for the former Link V-Type acetabular cup was 94. 5% after 5 years, 88. 1% after 10 years and 71. 2% after 15 years. The ”Bad Bramstedt” cup showed a 5 year survivorship rate of 97. 9%. Migration greater than 3 mm or tilting of the cup greater than 5 degrees was seen in 73% of the former type and in 39% of the modified cup. Radiolucent lines greater than 2 mm and detectable in two zones appeared in 6. 4% of the former Link V-Type and in 1. 7% of the ”Bad Bramstedt” cup design. Significant influence on cup migration was found in primary implant positioning and time elapsed. Due to the high rates of migration of the two implant designs and the frequent late aseptic loosening of the former Link V-Type acetabular component these two types of threaded cups were abandoned in favor of cementless press-fit cups.
Resection arthroplasty has been accepted as the treatment of choice for forefoot deformities in RA patients. Recent advance of drug therapy against RA encouraged us to preserve the joint in correction of forefoot deformities. Our technique aimed at preservation of the function of the MTP joints and is suitable for mild deformities in which only one or two rays are involved. Furthermore it is easy to correct the deformity of spray foot and reduce the plantar prominence of metatarsal head. This study revealed the good clinical result in short term follow-up. Although the long term result must to be waited, this method is one of recommendable options for RA patients with forefoot deformities.
To study whether intra-articular triamcinolone hexacetonide (iaTH) for the treatment of coxitis in patients with juvenile rheumatoid arthritis (JRA) causes femoral head necroses (FHN).
Fifty consecutive patients with JRA and coxitis were studied prospectively. Forty-eight children received iaTH in sixty-seven arthritic hips. The remaining two children exhibited three cases of femoral head necrosis at the initial assessment and were only followed; both were receiving long-term systemic steroids (LTSS). After a minimum of two years, the study was concluded with a final evaluation including MRI.
In thirty-nine of sixty-seven hip joints (58%), remission of the coxitis for a period of two years was obtained through a single administration of iaTH, another twelve hip joints went into remission after repeated TH injections (total remission rate = 76%). We observed two cases of femoral head necrosis (FHN) following iaTH. Both children were receiving LTSS. During the period between onset of JRA and screening assessment for this study, the children exhibited 2. 4 cases of FHN per 100 patient years vs. 1. 5 cases of FHN per 100 patient years between iaTH treatment and final follow-up. All five observed cases of FHN occurred among the twenty children who received LTSS, whereas no necrosis occurred in the thirty children who did not receive systemic corticosteroids (PÊ=Ê0. 009 Fisher’s Exact Test).
IaTH for juvenile rheumatoid coxitis was an effective treatment which did not increase the rate of FHN. Systemic steroids, however, (or their co-variable, severity of JRA) do increase the risk of FHN in JRA.
Overall outcome of bilateral hip and knee arthroplasty in the same patient with special regard to scheduling, postoperative complications and follow-up under consideration of the underlying disease.
More than 6000 primary THA and 5500 primary TKA were implanted at Schulthess Clinic since 1985, 8% of which in rheumatoid patients. Quadruple THA and TKA was performed in a total of 51 rheumatoid patients. Mean follow-up for knees was 8. 5 years (1–17), and 9. 5 years (1–18) for hips. 67% of implants were uncemented. In 21% of patients, all four prostheses were implanted within one year and in over 50% within a five year period.
Taking revision of components as failure there were three infections (CLS hip, GSB and LCS knee), two aseptic loosenings (Endler cup, GSB knee), two recurrent hip dislocations, three knee bearing exchanges (LCS, INNEX), and four patella component removals (GSB, PCA).
Quadruple arthroplasty in the lower extremity showed no increase of failure rate compared to single or dual arthroplasty patients. The results of this study support the indication for quadruple procedure with early postoperative rehabilitation and full weight bearing. Data suggest a procedure with hips before knees and at least two weeks between arthroplasty operations.
All 24 operations were performed by a deltopectoral approach with 11 longitudinal osteotomies of the clavicula, 12 osteotomies of the lesser tubercle, two osteotomies of the greater tubercle and two osteotomies of the coracoid process; all without complications. Seven times a cancellous bone graft of the glenoid was performed. A rotatorcuff rupture was seen five times; in all cases this was closed primarily. A rotatorcuff release was performed four times. Two procedures were complicated: one longitudinal fissure of the humerus and one fractured greater tubercle, both in the Biomet-group. The after-treatment for all shoulder arthroplasties was functional with use of a collar ‘n cuff accompanied by intensive physiotherapy with increasing load of use.
The purpose of this study was to determine whether internal mal-rotation of the femoral component is associated with arthrofibrosis in TKA. Multiple etiological factors have been suggested, but specific causes have not been identified. We hypothesized arthrofibrosis may be triggered by a combination of non-physiological kinematics (femoral component internal rotation) and a tight medial compartment.
From a consecutive cohort of 3058 mobile bearing TKA forty-four (1. 4%) cases were diagnosed as having arthrofibrosis, of which thirty-eight (86%) cases could be recruited. Thirty-eight patients with a well functioning TKA served as matched controls. Evaluation included CT investigation to determine femoral component rotation with reference to the transepicondylar axis (TEA).
Femoral components in the AF group were significantly (p< 0. 00001) internally mal-rotated by a mean of 4. 7 degrees ranging from ten degrees internal rotation (IR) to one degree external rotation (ER). Mean femoral rotational in the control group was parallel (0. 3 degrees IR) to the TEA (six degrees IR to four degrees ER). Arthrofibrosis was not associated with age, gender, body-mass-index, or preoperative diagnosis.
There is a highly significant association between arthrofibrosis in TKA and internal mal-rotation of the femoral component. On the base of these results it was hypothesized that non-physiological kinematics in TKA with mal-aligned femoral components influence and/or trigger arthrofibrosis in TKA.
In TKA with arthrofibrosis, we now consider femoral CT evaluation with the view to surgically rebalancing the flexion gap and realigning the femoral component, when internal mal-rotation is confirmed.
*This study has been cleared by the Ethical Committee, University of Zurich, Switzerland.
Correction of fixed valgus is a challenge in primary TKA. Achieving patello-femoral and femoral-tibial stability requires superficial/deep lateral side releases if non-constrained prostheses are utilized. The medial approach has disadvantages with more reported complications. The direct lateral approach, with/without tubercle osteotomy, is an approach option utilized in two reporting centers.
255 valgus TKAs with 5- to15-year follow-up were reviewed. Demographics included 91% females, 15% rheumatoid, mean age 69. Prostheses utilized were LCS mobile-bearing (meniscal PCL-retaining/rotating PCL-sacrificing). Patella was non-resurfaced in 90%; cement-less fixation in 86%. The direct lateral approach with similar lengthening techniques was used with tubercle osteotomy in one center and osteo-periosteal joint exposure in another.
Good/excellent 91%, modified HSS score improvement 57 to 85. Deformity (12) improved < 8 to 12 points (> 15o valgus to < 5o valgus). ROM improved from mean 11o/97o to 1/110o latest. Technical/prosthetic-related complications included: 7 bearing failures (5 meniscal, 2 rotating platform), 2 aseptic loosenings (tibial), 1 patella ligament rupture and 2 screw loosenings in the osteotomy group, 1 patella re-dislocation in a 75-year-old female with dislocation since age 15 (non-osteotomy group), 2 infections, and 1 re-operation for arthrofibrosis.
Valgus TKA using LCS moveable bearings implanted via a direct lateral approach are highly successful regarding stability and patella tracking. Failures correlate with inadequate/de-stabilizing releases and meniscal PCL-retaining prostheses. Rotating bearings allow for better stability and self-adjustment of common mal-rotation variables. The lateral approach allows for direct (stepwise) lengthening releases, improved patellar tracking, and precise gap balancing.
Patellectomized knees perform poorly with respect to extensor mechanism function and anterior knee pain. The clinical outcome after total knee arthroplasty (TKA) in this group of patients is inferior to patients with a patella independent of resurfacing.
To evaluate clinical long-term outcome, isokinetic strength and radiographic appearance of a neo-patella in TKA, which was reconstructed using autologous bonegraft.
In the period of 1990 to 1995, nine previously patellectomized patients with a mean age of 55 years (range: 38 to 67) underwent cementless Low-Contact-Stress TKA for osteoathritis of the tibio-femoral joint. One patient deceased 5 years post surgery. Mean follow-up was 8. 0 years (range: 6 to 12) The autograft was taken in five cases from the iliac crest, in two cases from the posterior femoral condyle and in another two cases from the opposite patella at time of simultaneous bilateral TKA surgery. Evaluation included clinical investigation, specific patella score, radiographic analysis and isokinetic strength measurement at 60 degrees per second (Biodex).
Clinical scores had a mean of 27 out of 30 points (range: 19 to 30) and mean isokinetic strength of knee extension reached 71Nm (81%) compared with the opposite site. One patient with bilateral patellectomy and unilateral TKA showed an increase of 50 % strength (51Nm versus 77Nm) in the kne with TKA and neo-patella. Radiographs in three planes showed minor signs of neo-patella bone resorption in three cases, but evidence of retrabeculation and bone remodelling in all neo-patellae.
Reconstruction of a neo-patella in TKA using autograft provides near to normal isokinetic strength, no evidence of considerable autograft resorption, excellent or good clinical outcome and high patients satisfaction after a mean of 8 years. The study provides encouraging data for reconstructing a neo-patella in TKA with autograft.
Accepted landmarks for determining femoral component rotation in total knee arthroplasty (TKA) include the posterior condyles, Whiteside’s line, arbitrary three to four degrees of external rotation, and transepicondylar axis (TEA). All methods require anatomical identification, which may be variable. The purpose of this study was to radiologically evaluate femoral component rotation (CT analysis) based on a method that references to the tibial shaft axis and balanced flexion tension without identification of femoral anatomical landmarks.
Out of a cohort of 3058 mobile bearing low contact stress TKA, CT scans of 38 randomly selected well functioning TKA were evaluated to determine femoral component positioning. Spiral CT scans of the femoral epicondylar region with four mm cuts were performed to accurately identify medial and lateral femoral epicondyles. Rotational alignment was measured in relation to the transepicondylar axis using CT-implemented software by two independent radiologists.
Mean femoral rotational alignment was parallel to the TEA (average 0. 3 degrees internal rotation) ranging from six degrees internal to four degrees external rotation. All thirty-eight cases had satisfactory clinical results, range of motion of over 90°, and showed perfect patello-femoral tracking and patellar congruency on axial views.
Femoral rotation position based on tibial shaft axis and balanced flexion tension gap is patient specific, reproducible and results in predictable femoral rotational positioning and patella tracking. CT analysis in this study confirms that the tibial shaft axis method produces a consistent femoral component positioning that relates accurately to the TEA. Tibial shaft axis method avoids the need for arbitrary landmark identification, placing the femoral component predictably in an optimum position in relation to the tibia and patella.
The purpose of this study was to determine whether internal mal-rotation of the femoral component is associated with arthrofibrosis in TKA. Multiple etiological factors have been suggested, but specific causes have not been identified. We hypothesized arthrofibrosis may be triggered by a combination of non-physiological kinematics (femoral component internal rotation) and a tight medial compartment.
From a consecutive cohort of 3058 mobile bearing TKA forty-four (1. 4%) cases were diagnosed as having arthrofibrosis, of which thirty-eight (86%) cases could be recruited. Thirty-eight patients with a well functioning TKA served as matched controls. Evaluation included CT investigation to determine femoral component rotation with reference to the transepicondylar axis (TEA).
Femoral components in the AF group were significantly (p< 0. 00001) internally mal-rotated by a mean of 4. 7 degrees ranging from ten degrees internal rotation (IR) to one degree external rotation (ER). Mean femoral rotational in the control group was parallel (0. 3 degrees IR) to the TEA (six degrees IR to four degrees ER). Arthrofibrosis was not associated with age, gender, body-mass-index, or preoperative diagnosis.
There is a highly significant association between arthrofibrosis in TKA and internal mal-rotation of the femoral component. On the base of these results it was hypothesized that non-physiological kinematics in TKA with mal-aligned femoral components influence and/or trigger arthrofibrosis in TKA.
In TKA with arthrofibrosis, we now consider femoral CT evaluation with the view to surgically rebalancing the flexion gap and realigning the femoral component, when internal mal-rotation is confirmed.
*This study has been cleared by the Ethical Committee, University of Zurich, Switzerland.
Thrombospondin-1 (TSP-1) a trimeric heigh-molecular weight glycoprotein is a multifunctional extra-cellular matrix protein. TSP-1 is involved in cell-matrix interactions of a various tissues. TSP-1 can bind to cells via different TSP-1 domains, its main receptors are CD 36 and CD51 (avb3-integrin). Nothern and western analysis showed the expression of TSP-1 in human cartilage, but its cellular source as well as the presence of its receptors CD36 and CD51 in normal and osteoarthritic cartilage are totally unknown.
We investigated 7 normal and 23 osteoarthritic cartilage samples on the expression patterns of TSP-1, CD36 and CD51, by immunohistochemistry and in situ hybridization.
In normal cartilage we found TSP-1 to be present in the middle and upper deep zone. Predominantly chondrocytes of the middle zone showed RNA-expression. Also, its receptor CD36 was found mainely in the chondrocytes of the superficial and middle zone. In moderate osteoarthritic cartilage we found an increased number of TSP-1 expressing chondrocytes, as well as an increased pericellular immunostainig quite near to the surface. However, a small number of CD36 positive cells were observed across the whole OA cartilage. In severe osteo-arthritic cartilage were observed a strong decrease in TSP-1 synthesizing chondrocytes by in situ hybridization as well as a strong reduction in the immunohistochemically matrix staining. In contrast to the decrease in TSP-1 we observed in 5 out of 8 these samples a overall enhanced number in CD 36 stained chondrocytes. Further, osteophytes with strong TSP-1 expression showed a large number of CD36 positive cells. However, CD51 positive chondrocytes could not be detected.
TSP-1 and its receptor are expressed in normal and osteoarthritic cartilage. The source of TSP-1 in normal cartilage are the middle zone chondrocytes, which also express the CD36-receptor. In early osteoarthritic cartilage an increase of TSP-1 was observed, whereas in later osteoarthritic cartilage TSP-1-synthesis is strongly decreased. It can be hypothesized that the strong enhanced number of CD36-stained chondrocytes in severe OA cartilage is a sign of chondrocytes frustrate efforts to contact the ECM, by binding to TSP-1.
Accepted landmarks for determining femoral component rotation in total knee arthroplasty (TKA) include the posterior condyles, Whiteside’s line, arbitrary three to four degrees of external rotation, and transepicondylar axis (TEA). All methods require anatomical identification, which may be variable. The purpose of this study was to radiologically evaluate femoral component rotation (CT analysis) based on a method that references to the tibial shaft axis and balanced flexion tension without identification of femoral anatomical landmarks.
Out of a cohort of 3058 mobile bearing low contact stress TKA, CT scans of 38 randomly selected well functioning TKA were evaluated to determine femoral component positioning. Spiral CT scans of the femoral epicondylar region with four mm cuts were performed to accurately identify medial and lateral femoral epicondyles. Rotational alignment was measured in relation to the transepicondylar axis using CT-implemented software by two independent radiologists.
Mean femoral rotational alignment was parallel to the TEA (average 0. 3 degrees internal rotation) ranging from six degrees internal to four degrees external rotation. All thirty-eight cases had satisfactory clinical results, range of motion of over 90°, and showed perfect patello-femoral tracking and patellar congruency on axial views.
Femoral rotation position based on tibial shaft axis and balanced flexion tension gap is patient specific, reproducible and results in predictable femoral rotational positioning and patella tracking. CT analysis in this study confirms that the tibial shaft axis method produces a consistent femoral component positioning that relates accurately to the TEA. Tibial shaft axis method avoids the need for arbitrary landmark identification, placing the femoral component predictably in an optimum position in relation to the tibia and patella.
In 1999, Insall developed new total knee system LPS-FLEXR mobile with Zimmer‘s corporation. This artificial knee joint has thicker posterior condyles, and has a polyethylene to prevent patellar tendon impingement. It allows an enlarged flexion angle, maximum one hundred fifty-five degrees. This prosthesis has a mobile bearing.
In addition to routine technique of arthroplasty, we want to add four points to achieve deep flexion. The first point is to make posterior clearance. The second point is to use a tension meter for soft tissue balancing. The third point is to gain a flexion gap as same as the extension gap by cutting posterior condyles of femur. The fourth point is to close retinaculum in flexion position.
We performed 17 total knee arthroplasties of 15 gonarthrosis patients with LPS-FLEXR mobile from January 2000 to March 2001. The 3 male and 12 female patients average age was 76 (range:62–87). We evaluated the clinical symptoms and the range of motion.
Postoperatively all patients had no pain in walking, no complications, and no component troubles. The range of motion in flexion of all patients averaged 138 degrees preoperatively, and 135 degrees postoperatively. The maximum flexion angles of 6 knee joints were over 145 degrees.
This implant should be designed to be suited to a deep flexion. However, the long term results should be followed in future.
The clinical and radiographic results of 172 patients with inflammatory arthropathies, mostly rheumatoid arthritis, were evaluated regarding to soft tissue problems, the type of destruction, and radiographic findings.
The frequency of early complications (n=11) and revisions (n=25) reflects the high morbidity of rheumatoid patients. Patient rated themselves as satisfied in 90%. The preoperative status of 26/100 points (34% adjusted score) improved to 56 points (73% adjusted score).
The effect of joint replacement on muscle strength (5/25 points) and active mobility (25/40 points) was limited because of the high frequency of rotator cuff tears and muscle atrophy. The active elevation improved from preoperatively 79° to 120° (gain 41+/−4°) on average. The radiographic analysis of the cemented stems revealed in three cases (2%) a migration and radiolucency lines in 24 cases (15%). The glenoid components showed in 70% radiolucency lines, which were progressive in 53%. In 5% a migration could be observed.
For reconstructive surgery of the deteriorated rheumatoid MCP-joints silastic implants are used in general. Though realignment and stability after silastic joint replacement is achieved many disadvantages as reduced ROM, fractures and osteolysis are known. The first study of the cement less, non-constrained MCP-arthroplasty with HM-prosthesis showed a high rate of subluxation and synovitis.
Therefore the design of the HM-prosthesis was changed with a PE-head to avoid wear and an increase of the diameter of the phalangeal base of 30% to get more stability.
In prospective study we replaced 20 MCP joints in RA with this new designed prosthesis.
short-time results after a mean Fu-period of 6 month (2–12 month) are now reported. In all cases a total replacement was performed. Clinical and radiographic re-examination could performed in all cases.
In all cases we found an osteo-integration, no infection was seen. A luxation or subluxation as we have seen in the old design was not seen in any new designed prosthesis. In all cases pain-reduction was reported. The range of motion improved in all cases (flexion/extension 70/5/0).
The results after changing the design of the HM-pros-thesis show an improvement of stability and show no wear, luxation or subluxation. The Improvement of mobility and pain-reduction is still seen as published in our studies before.
This first results have to be verified by longer FU-periods a higher number of patients.
Synovitis of the smaller hand joints leads to soft-tissue and bony affections. Radiologically Larsen/Dale/Eek (LDE) distinguish 6 stages of increasing destruction. Tendon ruptures, swan-neck and buttonhole deformities may occur. In early stages, when the ligament- and capsule structures require no balancing therapy, arthroscopic synovectomy may be indicated in order to prevent fast deteriorating of the joints and disability. We perform the endoscopic procedure in the MCP- and PIP-joints, when an oligoarticular situation is present or single digits are affected, provided that the surrounding soft tissues are intact, in LDE-stages 0 to 2/3. We use the laser additionally for completion of the synovectomy and for shrinking of the capsule.
Technically it is necessary to have an short optical device of 1. 0 diameter, miniaturised instruments, shaver and the laser at one’s disposal. The radial and the ulnar incision proximal to the joint are used.
A pilot study of 12 patients with an arthroscopic, laser-assisted synovectomy in 20 joints of various digits (LDE 0 – 2) are opposed to 10 patients with an open synovectomy of 24 joints. The follow-up-period amounts to 9 months (6 – 9). We have looked after the reccurrence rate, the time-lag until the patients are pain-free, the necessary rehabilitation measures, the progression of the LDE-stages, and the subjective judment of the patients.
Both groups had no recurrence of the synovitis in the joints cared for surgically. The period until the patients were free of complaints in the arthroscopic group amounts to 4 days, opposed to 10 days in the open surgery group. Radiologically both groups revealed no further bony destruction according to LDE. 12 physiotherapy treatments after open synovectomy are twice the amount needed for the endoscopic group. This is true also for the time away from work: 14 days against 7 days. The arthroscopically treated patients remark favorably the discrete scars, the relatively pain-free perioperative period, low tissue trauma, quick rehabilitation. In open surgery the patients complain about large scars and long postoperative swelling of the joints.
We can not guarantee the completeness of the synovectomy in both procedures. The effect of the intraoperative lavage and the assistance of the laser are not entirely clear either. The arthroscopic synovectomy itself is technically easy to perform. Although in this pilot study we have small numbers only, the results suggest that arthroscopic synovectomy is low in tissue trauma, quick in rehabilitation, perfect in patient acceptance and followed by a very short time away from work compared to open surgery.
The C-arm is routinely used introperatively to control the anatomic structures during osteotomies and during reposition and nailing of the femoral neck fractures.
Fluoroscopic navigation has been introduced in spinal surgery and it is a widely accepted tool for pedicel screws. It has been proven that fluoroscopic imaging in two planes shows an adequate reproduction of the 3-dimensional anatomy and enables a realistic acquisition for computer-assisted navigation.
This experience with the Medtronic system is now adapted for application as the „Viking System“ for total knee replacement using the Genesis II knee arthroplasty.
After experimental cadaver studies and critical evaluation the system was tested the first time in our clinic during live surgery. In the first series of 40 Genesis II TKR we could establish a high degree of accuracy and reproducibility with the fluoroscopic navigation. Several advantages using the fluoroscopic navigation can be shown:
The navigation offers an online documentation at each step during surgery These data give a good background for further studies Fluoroscopic assisted navigation needs only very short radiation exposure Fluoroscopic imaging is superior to virtual pixels in other systems There is no limitation to use fluoroscopic navigation in case of severe destruction of the knee or in case of severe contracture of the ipsilateral hip or ankle joint The intraoperative and postoperative controls show a deviation of the alignment of less than 2 degrees.
During the study we could find a reduction of the time of surgery. The examination of additional laxity tests at various degrees of flexion with the trial implants in situ give an assessment of the ligament stability.
Fluoroscopic assisted navigation may be used during the routine TKR to be prepared for the difficult case and to avoid malalignment in the routine TKR.
Further investigation i. e. in a prospective study may reveal the advantage of navigation in correlation to the clinical outcome and the survival rates of the TKR.
There is an incidence of failures of total wrist arthroplasties. We review our experiences in revising total wrist implant arthroplasties to arthrodeses. The most common mode of failure of the arthroplasties in our series was metacarpal loosening with dorsal perforation of the stem.
We used for the revision arthrodesis in all our cases tricortical iliac crest bone grafts and additional spongiosa transplants from this donor site region. In one case we used a vascularized iliac crest bone graft to bridge the bone defect because of a bad host quality of the recipient area. Fixation was achieved with plates and screws.
Our average follow-up period was 28 month. 14 patients with 15 failed wrist implants were treated with this technique. 14 patients undergoing arthrodesis attained a solid painless fusion after a single operation. In one case a non-union with a loosening of the screws due to using a non-rigid plate was seen. In this case a revision was necessary to achieve a bone healing. All patients were pain free and achieved an increased grip strength after bony fusion.
Arthrodesis after failed total wrist arthroplasty is a satisfactory salvage procedure even in cases with a bad quality of the recipient area. We recommend a rigid fixation technique to prevent non-unions.
Rheumatoid Arthritis (RA) is the most frequent inflammatory rheumatic disease. At the beginning of the disease, where after today‘s knowledge the therapeutic possibilities are largest, the diagnostic methods do not permit a differentiated estimation of the prognosis. Conventional x-rays are mostly normal and serum markers unspecific. So far – in contrast to other diseases – only few information has been drawn from the pathomorphologic substrate “synovium” itself to assess the prognosis. Reasons therefore are found in difficulties in obtaining synovial tissue without surgical intervention, particularly in patients with early arthritis.
By minimalizing the diagnostic instruments and improvement of the technique, nowadays synovial tissue sampling in RA has become minimal invasive and even possible from smallest joints, such as finger joints. Hereby, synovial analysis is open for detecting pathways of inflammation and joint destruction, which might support the advancement of new therapeutic strategies, followed by a better prognosis and outcome of RA.
The periprosthetic loss of bone mass may compromise the longevity of femoral stems in THA. The benefit of metaphyseal hydroxyapatite - coating remains controversial. Better Osseo integration is reported by Jaffe and Scott, whereas Dorr considered no clinical or radiographic value for the use of hydroxyapatite.
Evaluating the influence of this hydroxyapatite - coating of the femoral stems a double blind, randomized prospective study with two groups of uncemented total hip replacements using the Endoplus-SL-Plus-stem was conducted. Matched pairs with and without hydroxy-apatite-coating were compared clinically, radiographically and by QDR-bone-densitometry for 5 years with an average follow-up of 3, 7 years. 92 new hydroxylapatite-coated titanium stems and 90 non-coated stems were implanted. Main indications were an osteoarthritic (primary osteoarthritis / hip dysplasia / femur head necrosis: n = 134 (73, 6%) destruction or a postinflammatory arthritic destruction due to a rheumatoid arthritis (n = 48 ( 26, 4%))
The HA-coated stems showed a statistical significant increase in bone mineral density in Gruen zone 1 (789 g/cm2 vs. 711 g/cm2
The titanium/hydroxyapatite-coating enables a better early osteointegration of the
Nowadays, longevity of total knee arthroplasties is very acceptable. Survivorship analyses demonstrate a success in a range of 80% to more than 95% over a period of more than ten years (1–4). However, long-term results largely depend, amongst other factors, on restoration of physiological alignment of the lower limb (5–11). Jeffery et al. (12) reported a three percent loosening rate over eight years when knees were correctly aligned whereas insufficient alignment lead to prosthetic loosening in 24 percent. Rand and Coventry (13) found a 90 percent survivorship rate at ten years when the mechanical axis was aligned in a range from nought to four degrees of valgus. Valgus position of more than four degrees or varus alignment resulted in only 71 percent and 73 percent of survivorship respectively.
Recently, computer aided instrumentation systems (14,15) became available and preliminary results of small series were reported (16–17).
The purpose of this study was to assess the accuracy of computer integrated instrumentation for knee alignment.
The OrthoPilot® represents a computer controlled image supported alignment system. A 3-D Optotrak™ camera localizes infra-red diodes fixed to rigid bodies within the surgical field. Thereby a spatial coordinate reference system is provided. The localizer is linked to a UNIX work station which performs the operative protocol using a graphical interface and a foot pedal. The rigid bodies are fixed to the bones by bicortical screws. An intraoperative kinematic analysis and various additional landmarks lead to definition of the centres of hip, ankle and knee joint and sizing of endoprosthetic components. With the use of LED-equipped alignment instruments the femoral and tibial resection planes are determined.
The OrthoPilot® navigation system is not dependant on CT data and no additional preoperative planning is therefore necessary.
A prospective comparative multicentre study in five institutions, four in Germany and one in France, was carried out. 821 patients with primary tricompartimental knee arthroplasty using the SEARCH LC knee (B|Braun AESCULAP) were included in the study. The OrthoPilot® Navigation system was used in 555 cases and 266 knees were implanted with the use of conventional instrumentation. At the three months follow-up alignment was assessed using standardized one leg stance radiographs with regard to the mechanical axis and the femoral and tibial angels in the coronal plane. For the lateral femoral and tibial angels standard lateral x-rays were used. Prosthetic alignment was verified by an independent observer.
The radiographically assessed results were subdivided into three groups. An error of ± one degree in the radiographical measurements and small deviations caused by the play of surgical instruments have to be considered. With respect to the femoral and tibial angels in the ap and lateral view the group of very good clinical results was, therefore, defined in the range between ninty degrees and ± two degrees. Deviations of three and four degrees from the optimum were classified as being clinically acceptable. Aberrations of more than four degrees were classified as outliers. When measuring the mechanical axis deviations from fully precise femoral and tibial angels may add up. For this reason zero degrees ± three degrees were rated as a very good result, deviations of four to five degrees were considered to be acceptable and alignment beyond five degrees from the optimum was classified as an unsatisfactory result.
35. 2% of the navigated cases were aligned at exactly zero degrees. This was achieved in only 24. 4% of the manual cases. 88. 6% of cases using navigation and 72. 2% in the manual group showed zero degrees and varus or valgus angles of up to three degrees. 8. 9% and 18. 1% of cases respectively showed deviations of four or five degrees of valgus or varus alignment representing an acceptable clinical result. In only 2. 5% of the navigation group aberrations of more than five degrees occurred. The rate of dissatisfying results was 9. 8% in the manual group.
In the navigation group 48. 1% of cases showed an alignment at exactly 90 degrees which was the case in only 33. 5% of the control group. Altogether, in 89. 4% of the navigated cases a very good result was observed. In the conventionally instrumented cases only 77. 1% very good results were found. There were 1. 6% outliers beyond the limits of four degrees in the navigation group in comparison to 4. 9% amongst the control cases.
Very good results with up to two degrees of deviation from a ninety degree position were obtained in 75. 5% of navigated cases and 70. 7% of manual cases. 37. 3% and 34. 6% respectively showed an ideal alignment of exactly ninety degrees. Unsatisfactory results were observed in 9. 5% of the navigated cases and 9. 4% of the manual cases.
58. 7% of the computer assisted and 40. 6% of the reference cases were exactly aligned at rectangles. All in all, in 91. 9% navigated and only 83. 5% manual cases a very good result was obtained. Only 1. 1% outliers had to be observed in the navigation group whereas 3. 4% unsatisfactory results were registered with manual technique.
44. 3% of the navigated cases and only 26. 7% of cases in the control group were aligned perpendicular to the dorsal tibial cortex, thus showing no posterior slope. Altogether, 81. 3% could be classified as very good clinical results in the computer assisted group. The corresponding rate of the manual group was 69. 9%. Equivalent values of 8. 6% in the navigation group and 8. 3% in the reference group were registered beyond the limits of four degrees deviation.
The additional operation time for the use of the navigation system is calculated between eight and ten minutes after having passed through the learning curve.
Knee navigation facilitates proper alignment of endoprosthetic components and with the use of the Ortho-Pilot® system results are clearly more favourable in comparison to conventional instrumentation technique. In addition, the data obtained from literature demonstrate that the use of this navigation system contributes to reducing outliers in number. With the learning curve the OrthoPilot® alignment system proved to gain in reliability.
Deviations from perfect alignment are still difficult to be classified into surgical or technical deficiencies.
Many technical and software improvements which were introduced in the meantime will, in addition, contribute to reliability and time saving.
Comparative studies with different navigation systems are not yet available. They might allow an even more profound insight into the possibilities and advantages or disadvantages of computer assisted knee alignment.
(1) Knutson K, Lindstrand A, Lidgren L. Survival of knee arthroplasties, a nation-wide multicenter investigation of 8000 cases. J Bone Joint Surg. 1986; 68B: 795-803
(2) Scuderi GR, Insall JN, Windsor RE, Moran MC. Survivorship of cemented knee replacement. J Bone Joint Surg. 1989; 798-409
(3) Nafei A, Kristensen O, Knudson HM, Hvid I, Jensen J. Survivorship analysis of cemented total condylar knee arthoplasty. J Arthoplasty 11, 1996;07-10
(4) Ranawat CS, Flynn WF, Saddler S, Hansraj KH, Maynhard MJ. Long-term results of total condylar knee arthroplasty. A 15-years survivorship study. Clin Orthop 1993; 286:94-102
(5) Lotke PA, Ecker ML. Influence of positioning of prosthesis in total knee replacement. J Bone Joint Surg 1977;59-A:77-79
(6) Hood RW, Vanni M, Insall JN. The correction of knee alignment in 225 consecutive total condylar knee replacements. Clin Orthop 1981;160:94-105
(7) Bargren JH, Blaha JD, Freeman MAR. Alignment in total knee arthroplasty. Clin Orthop 1983;173:178-183.
(8) Hvid I, Nielsen S. Total condylar knee arthroplasty. Acta Orthop Scand 1984;55:160-165
(9) Tew M, Waugh W. Tibial-femoral alignment and the results of knee replacement. J Bone Joint Surg 1985;67-B:551-556
(10) Jonsson B, Astrom J. Alignment and long-term clinical results of a semi-constrained knee prosthesis. Clin Orthop 1988;226:124-128
(11) Ritter MA, Faris PM, Keating EM, Meding JB. Postoperative alignment of total knee replacement its effect on survival. Clin Orthop 1994;299:153-156
(12) Jeffery RS, Morris RW, Denham RA. Coronal alignment after total knee replacement. J Bone Joint Surg 1991;73-B:709-714
(13) Rand JA, Coventry MB. Ten-year evaluation of geometric total knee arthroplasty. 1988;232:168-173
(14) Leitner F, Picard F, Minfelde R, Schulz HJ, Clinquin P, Saragaglia D. Computer assisted knee surgical total replacement. In: CVRMed-MRCAS. Troccaz J, Grimson E, Mösges R (Eds). 1997; 630-638, Springer
(15) Delp SL, Stulberg SD, Davies BL, Picard F, Leitner F. Computer assisted knee replacement. Clin Orthop 1998; 354:49-56
(16) Picard F, Saragaglia D, Montbarbon E, Chaussard C, Leitner F, Raoult O. Computer assisted knee arthroplasty - preliminary clinical results with the Ortho-Pilot System. Abstract, 4th International CAOS Symposium, Davos, Switzerland, 1999
(17) Miehlke RK, Clemens U, Jens J-H, Kershally S. Navigation in der Knieendoprothetik - vorläufige klinische Erfahrungen und prospektiv vergleichende Studie gegenüber konventioneller Implantationstechnik, Z Orthop 2001; 139: 109-116
In 1994 Kofoed and Stürup already confirmed that within a follow-up of 10 years total ankle arthroplasty demonstrated a significant clinical improvement for the patients.
In recent studies a 12 – year survival rate even of 84% was described (Kofoed, 1995).
In a retrospective study we evaluated the short – and midterm results in 44 patients with unconstrained total ankle arthroplasty and cementless fixation. These ankle replacements were performed between 8/1997 and 12/2000. A critical assessment concerning the indications and contraindications of this arthroplasty was performed due to the fact, that this surgical technique is not yet mentioned as a routinely performed surgical procedure of the ankle. The advantages in comparison to the open or arthroscopically assisted arthrodesis of the ankle were described.
As initial diagnosis rheumatoid arthritis (n:16), post-traumatic osteoarthritis (n:10) or idiopathic osteoarthritis of the ankle (n:18) was mentioned. The patients age varied from 24 to 78 years; the 24 years old patient suffered from a posttraumatic osteoarthritis, in the 78 years old patient contralateral total ankle arthroplasty was performed 13 years ago.
There was a delay in superficial wound healing in 11 cases, in 4 cases soft tissue revision and once plastic surgery had to be performed. One female patient with RA had a postoperative deep infection after preoperative radiosynoviorthesis of the ankle.
Additionally osteosynthetical reconstruction of the fibula (n:2) and the talus (n:1) was necessary. One patient underwent revisional surgery due to progressive wear and fracture of the polyethylene inlay. Furthermore three patients suffered from continuing instability, that one had a secondary open arthrodesis and two a syndesmoplasty combined with revision of the PE inlay.
The radiological examination offered migration and progredient radiolucency lines especially near to the tibial part of the prosthesis in three cases.
Nevertheless more than 80% of the patients were satisfied or very satisfied with their ankle arthroplasty, only 4 patients now would have denied the surgical procedure. As main improvements reduction of pain and increased mobility (ROM: > 40°) were mentioned.
The success of total ankle arthroplasty may depend on exact technique, correct hindfoot alignment and sufficient capsuloligamentous stability of the ankle. So this surgical procedure may provide a high rate of functional improvement for the patients and may prevent the probably necessary arthrodesis.
The torsion of the humerus is defined as the angle between the axis of the humeral head and the axis of the trochlea humeri relative to the long axis of the humerus. In performimg shoulder arthroplasty it is an essential part of the procedure to restore the individual torsion. In some cases it might be difficult to detect the orignal border of the joint surface and thus the torsion. This situation occurs in severely destructed humeral heads as well as in fracture cases.
In the literature an average retrotorsion is given between 20–30 degrees, with a high standard deviation.
The aim of the following study was a critical analysis, if the sulcus intertubercularis can serve as an anatomical landmark for the orientation of humeral torsion in shoulder arthroplasty.
First, we defined the indivdual humeral torsion ( n = 40 ) by two independent anthropometric methods ( method according to Martin, method according to Knußmann).
Afterwards, the results of the measurements were compared to CT- scans taken by the same bones. The CT- measurements were performed by the method of Dähnert and Bernd, who used the midpoint of the humeral joint surface and the sulcus intertubercularis defining the proximal axis of retrotorsion.
Statitstical analysis was performed with varianz analysis, U-test according to Wilcoxon and Smirnov –Komolgorow test.
The anthropometric measurements according to Martin revealed an average retrotorsion of 23° degrees (+/− 9, 15 °). Comparing these data with the second anthropometric method ( according to Knuβmann) the measurements demonstrated a highly significant relationship( p < 0, 005).
The CT- measurements according to Dähnert showed an average of 53, 8° degrees ( +/− 8, 91°).
The different results were easy to explain because both methods used different bony landmarks.
Performing a varianz analysis the data showed a significant relationship ( p < 0, 05 ).
The average difference between the anthropometric – and the CT-measurements was 31 ° +/− 5, 93 ° degrees ( Minimum 14 °, Maximum 50°)
In severely destroyed shoulder joints it is sometimes difficult to identify the original anatomic borders of the joint surface. The reconstruction of the anatomical neck is the precondition to detect the individual retrotorsion performing a shoulder arthroplasty.
There are two options if that fails.
You may use an average retrotorsion of about 23 degrees or you may use the sulcus intertubercularis as an anatomical landmark. It only makes sense to use the Sulcus as an anatomical landmark, if there is a constant relationship between the orientation of the sulcus and the retrotorsion of the proximal humerus.
With our measurements we could demonstrate a close relationship between the sulcus and the orientation of the humeral joint surface, relative to the long axis of the humerus ( p< 0, 005 ).
The average difference between the anthropometric – and the CT-measurements was 31 ° +/− 5, 93 ° degrees ( Minimum 14 °, Maximum 50°). Using a standard head of 48 mm and adding the distance to the greater tubercle one should go about 10 mm lateral to the center of the sulcus intertubercularis. The distance varies with the head size.
The probability to match the individual torsion is higher using the sulcus intertubercularis as an anatomical landmark compared to the average retrotorsion.
Ultrasound screening has shown that the shoulder joint is almost always involved in rheumatoid arthritis. But only few of rheumatoid patients suffering from omarthritis are in considerable pain. Loss of strength and mobility is often compensated by the adjacent joints. Low patients demands, as pain and swelling can be treated often temporarely successfully by corticoid injections and the need of a wide exposure of the shoulder joint when performing an open synovectomy are the reasons of the low rate of synovectomies performed in rheumatoid shoulder joints. The clinical outcome after synovectomies in rheumatoid omarthritis is generally superior to those of knee synovectomies and shows a reliable reduction of pain, swelling and an increase of ROM. The surgical trauma in open synovectomy of the shoulder results in an impairment of the complex muscle co-ordination of the shoulder and a painful long-lasting aftertreatment. This disadvantages can be prevented when using arthroscopic techniques.
The advantages of the arthroscopic technique are mostly obvious in the shoulder joint. The reduced surgical trauma of the periarticular tissue leaving the proprioreception intact results in reduced postoperative pain, allowing early mobilisation and shorter rehabilitation.
Arthroscopic surgery of the shoulder is performed with the patient in beach- chair position under general anesthesia. We use a standard 5mm arthroscope and a motorised synovial resector. To prevent bleeding it is advantageous to utilise cooled non-ionic irrigation solution with epinephrin in addition pressurised by a roller pump. Synovectomy of the glenohumeral joint and of the subacromial bursa is performed via four portals. Potential hazards like injury to the periarticular vessels and nerves or damage of the joint cartilage especially in stiff shoulders can only be prevented with careful proceeding. Active and passive physiotherapy starts on the first postoperative day.
Our first series of 12 shoulder arthroscopies done 1989–1991 was followed 3. 8 years postoperatively. Swelling and pain at rest disappeared rapidly after surgery. Pain during motion took longer to subside. At the end of follow-up patients reported slight pain on motion in five shoulders. Postoperatively all patients reported improvement of pain. There was one recurrence of swelling due to bursitis. In this patient no bursectomy was done during shoulder arthroscopy, which is now done as a routine. There was subjectively and objectively an increase of strength postoperatively. ROM showed immediate postoperative improvement, although a slight reduction was noticed during the follow-up period.
In 1990–1999 we performed 52 arthroscopical synovectomies of rheumatoid shoulders. 31 shoulders could be followed by questionnaire at a mean of 6. 5years postoperatively. Pain at rest and pain on motion was improved in about 80% and 74% respectively. Recurrence of swelling was reported by 26% of the patients. Five patients has to be operated again. The clinical outcome compare favourably with the results published about open shoulder synovectomy
Five patients with large humeral cysts were treated with arthroscopic synovectomy, arthroscopically assisted curettage and bone grafting of the cyst via a small incision at the major tuberculum. Until now none of the patients suffered from humeral collaps, no shoulder has to be replaced.
In painful rheumatoid omarthritis swelling and pain can be improved reliably with arthroscopic synovectomy. The reduced surgical trauma of minimal invasive synovectomy should raise the rate of early preventive surgery.
Severe acetabular bone stock loss compromises the outcome in primary and revision total hip arthroplasty. This acetabular deficienca occurs very often in Rheumatoid Arthritis.
In 1979 a biologic method was introduced with tightly impacted cancellous allograft in combination with a cemented polyethylene cup for acetabular reconstruction. With this technique it is possible to replace the loss of bone and restore hip function with a standard implant.
Because of the poor long term results and our own experience with large solid grafts we started in 1998 to use the impaction grafting in primary and revision hip replacements in Osteoarthritis and Rheumatoid Arthritis.
Between 1998 and 2001 35 acetabular reconstructions were performed in 29 patients with rheumatoid arthritis. 3 Patients were lost to follow up.
24 primary and 11 Revision Arthroplasties were performed. The average age was 55( 22-73. 29 female, 6 male.
58 Patients had additional dysplasia.
We had cavitary, segmental and also combined defects.
Femoral head autografts were used in all primaries, allografts were used in revision surgery.
Firstly the peripheral and central segmental defects were close with a metal mesh, so that only a cavitary defect remained. The cavity was filled with bone chips which were impacred layer by layer. To strabilize these reconstruction cement was used in direct contact with the graft.
In the Merle d’ Aubigne Score an improvement in pain, walking ability and function were observed. We had 1case of aseptic loosening, in a 73 year old female.
After 10 month the grafts were incorporated.
Our results are short term results- compared to the international literature ( Rosenberg et al. ) Nevertheless we can confirm the technique can be used with good results in cases with severe acetabular defects due to rheumatoid arthritis.
We evaluated the clinical results of Total Elbow Arthroplasties(TEA) that had been performed from Febrary 1986 through December 2001 in 95 patients. We used non-constrained, surface-arthroplasty prostheses (DOH type, MRCH type and Yamamoto elbow). The duration of follow up averaged 8 years(range 1 year to 13 years). 95 patients had rtheumatoid arthritis. There were 85 women and 10 men. Their mean age at surgery was 56 years. The results of TEA were evaluated according to range of motion, degree of pain, radiographical findings, patient‘s assessment and complications.
Post-operative arc of motion of the elbow (flexion, pro-nation and supination) improved from pre-operative arc of motion. 84% of elbows were pain-free. At the average 8 year follow-up, 80% of patients had satisfactory results clinically. The roentgenograms showed a radiolucent line adjacent to 32% of humeral and 15% of ulnar components. We experienced post-operative complications such as ulnar nerve palsies, radial nerve palsies, infections and dislocations.
In the framework of the modiCAS (Modular Interactive Computer Assisted Surgery) Project, which emerged from a collaboration of the University of Siegen and the University of Frankfurt in the fields of mechatronics and medicine, the development of a modular system to assist the surgeon during the whole planning and operation procedure has been started. A completely new realization of a planning system for bone surgery and alloarthroplasty is presented. Characteristics of the new system are generic interfaces for navigation, robotics and real-time data acquisition, graphic interactivity, documentation of each planning-step, a flexible wizard-guided concept and adaptable teaching modes. The system can be configured to any data source such as X-ray, CT, MRI, US with individual calibration. For planning, the data sources can be merged in any user defined way. In contrast to all existing planning systems the presented system can optionally be linked to navigation and robotic systems.
The software was realized to run platform-independent on any personal computer surrounding. We used commercially available software libraries for computer graphics and graphical user interface programming. The whole system consists of several modules which are closely linked together and support all major pre- and intraoperative steps of surgery. The user interface remains the same during the planning and the intervention. Preoperative planning is carried out on a totally new planning station comprising an interactive and intuitive graphic interface, while intraoperative features include interactive matching procedures, true real-time-capability and incorporation of navigation and robotics.
Initially we realized modules to support total hip allo-arthroplasty. The first application of the system is for a clinical trial on total hip alloarthroplasty. Planning is performed on the basis of radiographs and CT-datasets. Intraoperatively a navigation system and a robotic surgery system are used. Preliminary results show very precise and reproducible plannings that could be achieved in short time without special training of the clinician. Furthermore the unlimited intraoperative access to the whole planning dataset appeared to be very convenient to the surgeon because it allowed immediate response to unforeseen patient specific situations.
Future adaptations of the universal planning system will be total knee alloarthroplasty, spine surgery and trauma surgery. The existing system can easily be configured to any surgical procedure because the same basic functionality is used for all applications and only special configurative datasets have to be generated for each application.
The open architecture of the system enables easy integration of further input or output devices, an easy adaptation to different interventions, planning styles and operative techniques is possible.